Canonical Allele Identifier: CA775632391
Gene:

Linked Data

dbSNP Id: rs937717119

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137664G>A , CM000679.2:g.8137664G>A GRCh38
NC_000017.10:g.8040982G>A , CM000679.1:g.8040982G>A GRCh37
NC_000017.9:g.7981707G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1185G>A
XR_934203.1:n.70-1813G>A
XR_934202.2:n.414-1185G>A