Canonical Allele Identifier: CA862568025
Gene:

Linked Data

dbSNP Id: rs1450191826
MyVariant Identifiers: chr9:g.25551177T>G (hg19) chr9:g.25551179T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551179T>G , CM000671.2:g.25551179T>G GRCh38
NC_000009.11:g.25551177T>G , CM000671.1:g.25551177T>G GRCh37
NC_000009.10:g.25541177T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-607A>C
XR_929525.2:n.674-607A>C
Search 100 bp 5'
Search 100 bp 3'