Canonical Allele Identifier: CA832196425
Gene:

Linked Data

dbSNP Id: rs758509226

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.118519399G>A , CM000669.2:g.118519399G>A GRCh38
NC_000007.13:g.118159453G>A , CM000669.1:g.118159453G>A GRCh37
NC_000007.12:g.117946689G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927908.1:n.388+5572G>A
XR_927909.1:n.388+5572G>A
XR_927910.1:n.388+5572G>A
XR_927909.2:n.426+5572G>A