Canonical Allele Identifier: CA1462694321
Gene:

Linked Data

dbSNP Id: rs1756230325

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558319A>G , CM000666.2:g.62558319A>G GRCh38
NC_000004.11:g.63424037A>G , CM000666.1:g.63424037A>G GRCh37
NC_000004.10:g.63106632A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5525A>G