Canonical Allele Identifier: CA1181633475
Gene:

Linked Data

dbSNP Id: rs1652358024

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564045A>G , CM000663.2:g.94564045A>G GRCh38
NC_000001.10:g.95029601A>G , CM000663.1:g.95029601A>G GRCh37
NC_000001.9:g.94802189A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+432A>G