Canonical Allele Identifier: CA1674885478

Gene:

Linked Data

• dbSNP Id: rs1778853098

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812229G>A , CM000668.2:g.155812229G>A	GRCh38
NC_000006.11:g.156133363G>A , CM000668.1:g.156133363G>A	GRCh37
NC_000006.10:g.156175055G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+18810G>A
XR_943146.1:n.645-190C>T
XR_001744423.1:n.699-190C>T
XR_001744424.1:n.79+18810G>A