Canonical Allele Identifier: CA31701783
Gene:

Linked Data

dbSNP Id: rs79275492

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649365T>G , CM000663.2:g.168649365T>G GRCh38
NC_000001.10:g.168618603T>G , CM000663.1:g.168618603T>G GRCh37
NC_000001.9:g.166885227T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8090A>C
XR_922259.2:n.332-8090A>C