Canonical Allele Identifier: CA1181633470
Gene:

Linked Data

dbSNP Id: rs1652357852

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564036T>A , CM000663.2:g.94564036T>A GRCh38
NC_000001.10:g.95029592T>A , CM000663.1:g.95029592T>A GRCh37
NC_000001.9:g.94802180T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+423T>A