Canonical Allele Identifier: CA862161275
Gene:

Linked Data

dbSNP Id: rs1413716811
MyVariant Identifiers: chr9:g.21755958A>G (hg19) chr9:g.21755959A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755959A>G , CM000671.2:g.21755959A>G GRCh38
NC_000009.11:g.21755958A>G , CM000671.1:g.21755958A>G GRCh37
NC_000009.10:g.21745958A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11866T>C
Search 100 bp 5'
Search 100 bp 3'