Canonical Allele Identifier: CA1358881716
Gene:

Linked Data

dbSNP Id: rs2040646162

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263228C>G , CM000665.2:g.39263228C>G GRCh38
NC_000003.11:g.39304719C>G , CM000665.1:g.39304719C>G GRCh37
NC_000003.10:g.39279723C>G NCBI36
NG_016362.1:g.23508G>C

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2745C>G