Linked Data
ClinVar Variation Id:
1128000
ClinVar RCV Id:
RCV001460621
dbSNP Id:
rs1234807594
gnomAD v4:
13-20189219-G-T
MyVariant Identifiers:
chr13:g.20763358G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189219G>T , CM000675.2:g.20189219G>T | GRCh38 |
| NC_000013.10:g.20763358G>T , CM000675.1:g.20763358G>T | GRCh37 |
| NC_000013.9:g.19661358G>T | NCBI36 |
| NG_008358.1:g.8757C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.363C>A | ENSP00000372295.1:p.Ile121= | |
| ENST00000382848.5:c.363C>A MANE Select | ENSP00000372299.4:p.Ile121= | |
| ENST00000382844.1:c.363C>A | ENSP00000372295.1:p.Ile121= | |
| ENST00000382848.4:c.363C>A | ENSP00000372299.4:p.Ile121= | |
| NM_004004.5:c.363C>A | NP_003995.2:p.Ile121= | |
| XM_011535049.1:c.363C>A | XP_011533351.1:p.Ile121= | |
| XM_011535049.2:c.363C>A | XP_011533351.1:p.Ile121= | |
| NM_004004.6:c.363C>A MANE Select | NP_003995.2:p.Ile121= |