Canonical Allele Identifier: CA841571703
Gene:

Linked Data

dbSNP Id: rs1428012328

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146955G>T , CM000669.2:g.69146955G>T GRCh38
NC_000007.13:g.68611942G>T , CM000669.1:g.68611942G>T GRCh37
NC_000007.12:g.68249878G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-829C>A