Canonical Allele Identifier: CA168427889
Gene:

Linked Data

dbSNP Id: rs577113170

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.145144381G>T , CM000669.2:g.145144381G>T GRCh38
NC_000007.13:g.144841474G>T , CM000669.1:g.144841474G>T GRCh37
NC_000007.12:g.144472407G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928090.1:n.1968-12554G>T
XR_928090.2:n.4143-12554G>T