Canonical Allele Identifier: CA890857268
Gene:

Linked Data

dbSNP Id: rs1177489568

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649416T>G , CM000663.2:g.168649416T>G GRCh38
NC_000001.10:g.168618654T>G , CM000663.1:g.168618654T>G GRCh37
NC_000001.9:g.166885278T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8141A>C
XR_922259.2:n.332-8141A>C