Canonical Allele Identifier: CA1284431683
Gene:

Linked Data

dbSNP Id: rs923709995

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368953C>G , CM000664.2:g.122368953C>G GRCh38
NC_000002.11:g.123126529C>G , CM000664.1:g.123126529C>G GRCh37
NC_000002.10:g.122842999C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24010C>G
XR_001739684.1:n.556-24010C>G