Canonical Allele Identifier: CA188145849
Gene:

Linked Data

dbSNP Id: rs960010424
MyVariant Identifiers: chr9:g.1787468A>C (hg19) chr9:g.1787468A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787468A>C , CM000671.2:g.1787468A>C GRCh38
NC_000009.11:g.1787468A>C , CM000671.1:g.1787468A>C GRCh37
NC_000009.10:g.1777468A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68556A>C
Search 100 bp 5'
Search 100 bp 3'