Canonical Allele Identifier: CA1689218337
Gene:

Linked Data

dbSNP Id: rs1783120008

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400738A>G , CM000669.2:g.13400738A>G GRCh38
NC_000007.13:g.13440363A>G , CM000669.1:g.13440363A>G GRCh37
NC_000007.12:g.13406888A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90415A>G