Canonical Allele Identifier: CA1880834336

Gene:

Linked Data

• dbSNP Id: rs1829778250

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576800A>G , CM000671.2:g.129576800A>G	GRCh38
NC_000009.11:g.132339079A>G , CM000671.1:g.132339079A>G	GRCh37
NC_000009.10:g.131378900A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1202A>G