Canonical Allele Identifier: CA890857252
Gene:

Linked Data

dbSNP Id: rs1400035627

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649406T>A , CM000663.2:g.168649406T>A GRCh38
NC_000001.10:g.168618644T>A , CM000663.1:g.168618644T>A GRCh37
NC_000001.9:g.166885268T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8131A>T
XR_922259.2:n.332-8131A>T