Canonical Allele Identifier: CA1358881710
Gene:

Linked Data

dbSNP Id: rs1482588382

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263210G>C , CM000665.2:g.39263210G>C GRCh38
NC_000003.11:g.39304701G>C , CM000665.1:g.39304701G>C GRCh37
NC_000003.10:g.39279705G>C NCBI36
NG_016362.1:g.23526C>G

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2727G>C