Linked Data
dbSNP Id:
rs1398045350
gnomAD v2:
20-60503264-C-T
gnomAD v3:
20-61928206-C-T
gnomAD v4:
20-61928206-C-T
COSMIC:
COSM4670971
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.61928206C>T , CM000682.2:g.61928206C>T | GRCh38 |
| NC_000020.10:g.60503264C>T , CM000682.1:g.60503264C>T | GRCh37 |
| NC_000020.9:g.59936659C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614565.5:c.1788C>T MANE Select | ENSP00000484928.1:p.Ser596= | |
| ENST00000543233.2:c.1566C>T | ENSP00000443301.1:p.Ser522= | |
| ENST00000611855.4:c.1506C>T | ENSP00000480844.1:p.Ser502= | |
| ENST00000614565.4:c.1788C>T | ENSP00000484928.1:p.Ser596= | |
| NM_001252338.2:c.1677C>T | NP_001239267.1:p.Ser559= | |
| NM_001252339.2:c.1566C>T | NP_001239268.1:p.Ser522= | |
| NM_001794.4:c.1788C>T | NP_001785.2:p.Ser596= | |
| NM_001794.5:c.1788C>T MANE Select | NP_001785.2:p.Ser596= | |
| NM_001252339.3:c.1566C>T | NP_001239268.1:p.Ser522= |