Canonical Allele Identifier: CA54965470
Gene:

Linked Data

dbSNP Id: rs997392436

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368848A>G , CM000664.2:g.122368848A>G GRCh38
NC_000002.11:g.123126424A>G , CM000664.1:g.123126424A>G GRCh37
NC_000002.10:g.122842894A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24115A>G
XR_001739684.1:n.556-24115A>G