Canonical Allele Identifier: CA191701664
Gene:

Linked Data

dbSNP Id: rs1029573734
MyVariant Identifiers: chr9:g.25551102C>T (hg19) chr9:g.25551104C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551104C>T , CM000671.2:g.25551104C>T GRCh38
NC_000009.11:g.25551102C>T , CM000671.1:g.25551102C>T GRCh37
NC_000009.10:g.25541102C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-532G>A
XR_929525.2:n.674-532G>A
Search 100 bp 5'
Search 100 bp 3'