Canonical Allele Identifier: CA2702242685
Gene:

Linked Data

dbSNP Id: rs572989557

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263211T>C , CM000665.2:g.39263211T>C GRCh38
NC_000003.11:g.39304702T>C , CM000665.1:g.39304702T>C GRCh37
NC_000003.10:g.39279706T>C NCBI36
NG_016362.1:g.23525A>G

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2728T>C