Canonical Allele Identifier: CA1358881722
Gene:

Linked Data

dbSNP Id: rs1575204353

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263232T>C , CM000665.2:g.39263232T>C GRCh38
NC_000003.11:g.39304723T>C , CM000665.1:g.39304723T>C GRCh37
NC_000003.10:g.39279727T>C NCBI36
NG_016362.1:g.23504A>G

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2749T>C