Canonical Allele Identifier: CA1057529110
Gene:

Linked Data

dbSNP Id: rs1576940604

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931550A>G , CM000665.2:g.187931550A>G GRCh38
NC_000003.11:g.187649338A>G , CM000665.1:g.187649338A>G GRCh37
NC_000003.10:g.189132032A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1364T>C