Canonical Allele Identifier: CA861674110

Gene:

Linked Data

• dbSNP Id: rs1385575397
• gnomAD v3: 9-1787597-C-T
• gnomAD v4: 9-1787597-C-T
• MyVariant Identifiers: chr9:g.1787597C>T (hg19) ; chr9:g.1787597C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.1787597C>T , CM000671.2:g.1787597C>T	GRCh38
NC_000009.11:g.1787597C>T , CM000671.1:g.1787597C>T	GRCh37
NC_000009.10:g.1777597C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001746599.1:n.142+68685C>T