Linked Data
ClinVar Variation Id:
1352749
ClinVar RCV Id:
RCV002049536
dbSNP Id:
rs1269489339
gnomAD v2:
19-17937590-G-A
gnomAD v3:
19-17826781-G-A
gnomAD v4:
19-17826781-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17826781G>A , CM000681.2:g.17826781G>A | GRCh38 |
| NC_000019.9:g.17937590G>A , CM000681.1:g.17937590G>A | GRCh37 |
| NC_000019.8:g.17798590G>A | NCBI36 |
| NG_007273.1:g.26211C>T , LRG_77:g.26211C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526008.6:c.*1894C>T | ENSP00000513006.1:n.*1894C>T | |
| ENST00000696967.1:n.2514C>T | ||
| ENST00000696968.1:n.570C>T | ||
| ENST00000696969.1:n.2294C>T | ||
| ENST00000458235.7:c.3337C>T MANE Select | ENSP00000391676.1:p.His1113Tyr | |
| ENST00000458235.5:c.3337C>T | ENSP00000391676.1:p.His1113Tyr | |
| ENST00000527031.5:n.2279-1471C>T | ||
| ENST00000527670.5:c.3337C>T | ENSP00000432511.1:p.His1113Tyr | |
| NM_000215.3:c.3337C>T , LRG_77t1:c.3337C>T | NP_000206.2:p.His1113Tyr | |
| XM_005259896.2:c.3466C>T | XP_005259953.1:p.His1156Tyr | |
| XM_006722745.2:c.3337C>T | XP_006722808.1:p.His1113Tyr | |
| XM_005259896.3:c.3466C>T | XP_005259953.1:p.His1156Tyr | |
| NM_000215.4:c.3337C>T MANE Select | NP_000206.2:p.His1113Tyr |