Canonical Allele Identifier: CA188145844

Gene:

Linked Data

• dbSNP Id: rs1017776556
• MyVariant Identifiers: chr9:g.1787435C>G (hg19) ; chr9:g.1787435C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787435C>G , CM000671.2:g.1787435C>G	GRCh38
NC_000009.11:g.1787435C>G , CM000671.1:g.1787435C>G	GRCh37
NC_000009.10:g.1777435C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746599.1:n.142+68523C>G