Canonical Allele Identifier: CA191701660
Gene:

Linked Data

dbSNP Id: rs1004907578
gnomAD v3: 9-25551078-C-T
gnomAD v4: 9-25551078-C-T
MyVariant Identifiers: chr9:g.25551076C>T (hg19) chr9:g.25551078C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551078C>T , CM000671.2:g.25551078C>T GRCh38
NC_000009.11:g.25551076C>T , CM000671.1:g.25551076C>T GRCh37
NC_000009.10:g.25541076C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-506G>A
XR_929525.2:n.674-506G>A
Search 100 bp 5'
Search 100 bp 3'