Linked Data
ClinVar Variation Id:
1810101
ClinVar RCV Id:
RCV002508657
dbSNP Id:
rs1726221678
gnomAD v4:
4-88007744-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88007744C>A , CM000666.2:g.88007744C>A | GRCh38 |
| NC_000004.11:g.88928896C>A , CM000666.1:g.88928896C>A | GRCh37 |
| NC_000004.10:g.89147920C>A | NCBI36 |
| NG_008604.1:g.5077C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.11C>A MANE Select | ENSP00000237596.2:p.Ser4Tyr | |
| ENST00000237596.6:c.11C>A | ENSP00000237596.2:p.Ser4Tyr | |
| NM_000297.3:c.11C>A | NP_000288.1:p.Ser4Tyr | |
| XM_011532028.1:c.11C>A | XP_011530330.1:p.Ser4Tyr | |
| XR_244632.2:n.106C>A | ||
| NR_156488.1:n.98C>A | ||
| XM_011532028.2:c.11C>A | XP_011530330.1:p.Ser4Tyr | |
| NM_000297.4:c.11C>A MANE Select | NP_000288.1:p.Ser4Tyr | |
| NR_156488.2:n.110C>A |