Canonical Allele Identifier: CA54965477
Gene:

Linked Data

dbSNP Id: rs10496584

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368903A>G , CM000664.2:g.122368903A>G GRCh38
NC_000002.11:g.123126479A>G , CM000664.1:g.123126479A>G GRCh37
NC_000002.10:g.122842949A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24060A>G
XR_001739684.1:n.556-24060A>G