Canonical Allele Identifier: CA1704517777

Gene:

Linked Data

• dbSNP Id: rs1784762792

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.46032956A>G , CM000669.2:g.46032956A>G	GRCh38
NC_000007.13:g.46072554A>G , CM000669.1:g.46072554A>G	GRCh37
NC_000007.12:g.46039079A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745203.1:n.1270-3662A>G