Linked Data
ClinVar Variation Id:
3073200
ClinVar RCV Id:
RCV004015214
dbSNP Id:
rs886038322
gnomAD v4:
19-38573236-C-T
MyVariant Identifiers:
chr19:g.39063876C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38573236C>T , CM000681.2:g.38573236C>T | GRCh38 |
| NC_000019.9:g.39063876C>T , CM000681.1:g.39063876C>T | GRCh37 |
| NC_000019.8:g.43755716C>T | NCBI36 |
| NG_008866.1:g.144537C>T , LRG_766:g.144537C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.994C>T | ||
| ENST00000688602.1:c.2391C>T | ||
| ENST00000689936.1:c.2363C>T | ||
| ENST00000359596.8:c.14058C>T MANE Select | ENSP00000352608.2:p.Gly4686= | |
| ENST00000355481.8:c.14043C>T | ENSP00000347667.3:p.Gly4681= | |
| ENST00000359596.7:c.14058C>T | ENSP00000352608.2:p.Gly4686= | |
| ENST00000360985.7:c.14040C>T | ENSP00000354254.4:p.Gly4680= | |
| NM_000540.2:c.14058C>T , LRG_766t1:c.14058C>T | NP_000531.2:p.Gly4686= | |
| NM_001042723.1:c.14043C>T | NP_001036188.1:p.Gly4681= | |
| XM_006723317.1:c.14040C>T | XP_006723380.1:p.Gly4680= | |
| XM_006723319.1:c.14025C>T | XP_006723382.1:p.Gly4675= | |
| XM_011527204.1:c.14055C>T | XP_011525506.1:p.Gly4685= | |
| XM_011527205.1:c.13971C>T | XP_011525507.1:p.Gly4657= | |
| XM_006723317.2:c.14040C>T | XP_006723380.1:p.Gly4680= | |
| XM_006723319.2:c.14025C>T | XP_006723382.1:p.Gly4675= | |
| XM_011527205.2:c.13971C>T | XP_011525507.1:p.Gly4657= | |
| NM_000540.3:c.14058C>T MANE Select | NP_000531.2:p.Gly4686= | |
| NM_001042723.2:c.14043C>T | NP_001036188.1:p.Gly4681= |