Canonical Allele Identifier: CA31701794
Gene:

Linked Data

dbSNP Id: rs915574794

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649373C>T , CM000663.2:g.168649373C>T GRCh38
NC_000001.10:g.168618611C>T , CM000663.1:g.168618611C>T GRCh37
NC_000001.9:g.166885235C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8098G>A
XR_922259.2:n.332-8098G>A