Canonical Allele Identifier: CA31701769
Gene:

Linked Data

dbSNP Id: rs1000080054

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649341A>G , CM000663.2:g.168649341A>G GRCh38
NC_000001.10:g.168618579A>G , CM000663.1:g.168618579A>G GRCh37
NC_000001.9:g.166885203A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8066T>C
XR_922259.2:n.332-8066T>C