Canonical Allele Identifier: CA1704517826
Gene:

Linked Data

dbSNP Id: rs1784763854

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46033053G>A , CM000669.2:g.46033053G>A GRCh38
NC_000007.13:g.46072651G>A , CM000669.1:g.46072651G>A GRCh37
NC_000007.12:g.46039176G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3565G>A