Canonical Allele Identifier: CA188145895

Gene:

Linked Data

• dbSNP Id: rs944153450
• MyVariant Identifiers: chr9:g.1787704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787704C>A , CM000671.2:g.1787704C>A	GRCh38
NC_000009.11:g.1787704C>A , CM000671.1:g.1787704C>A	GRCh37
NC_000009.10:g.1777704C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746599.1:n.142+68792C>A