Canonical Allele Identifier: CA691969128
Gene:

Linked Data

dbSNP Id: rs1470163480

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004918G>A , CM000674.2:g.76004918G>A GRCh38
NC_000012.11:g.76398698G>A , CM000674.1:g.76398698G>A GRCh37
NC_000012.10:g.74684965G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1271C>T
XR_001749218.2:n.402+1271C>T
XR_945110.3:n.402+1271C>T