Canonical Allele Identifier: CA191701674
Gene:

Linked Data

dbSNP Id: rs745485673
gnomAD v3: 9-25551180-A-G
gnomAD v4: 9-25551180-A-G
MyVariant Identifiers: chr9:g.25551178A>G (hg19) chr9:g.25551180A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551180A>G , CM000671.2:g.25551180A>G GRCh38
NC_000009.11:g.25551178A>G , CM000671.1:g.25551178A>G GRCh37
NC_000009.10:g.25541178A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-608T>C
XR_929525.2:n.674-608T>C
Search 100 bp 5'
Search 100 bp 3'