Canonical Allele Identifier: CA890857304
Gene:

Linked Data

dbSNP Id: rs1397397337

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649477C>A , CM000663.2:g.168649477C>A GRCh38
NC_000001.10:g.168618715C>A , CM000663.1:g.168618715C>A GRCh37
NC_000001.9:g.166885339C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8202G>T
XR_922259.2:n.332-8202G>T