Canonical Allele Identifier: CA156301759
Gene:

Linked Data

dbSNP Id: rs748904003

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605915G>A , CM000669.2:g.26605915G>A GRCh38
NC_000007.13:g.26645534G>A , CM000669.1:g.26645534G>A GRCh37
NC_000007.12:g.26612059G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6545C>T
XR_927131.2:n.1186-6545C>T