Canonical Allele Identifier: CA2698910379
Gene:

Linked Data

dbSNP Id: rs2125216986

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843923C>G , CM000664.2:g.17843923C>G GRCh38
NC_000002.11:g.18025190C>G , CM000664.1:g.18025190C>G GRCh37
NC_000002.10:g.17888671C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3771G>C