Canonical Allele Identifier: CA191701670
Gene:

Linked Data

dbSNP Id: rs565770173
gnomAD v3: 9-25551128-T-C
gnomAD v4: 9-25551128-T-C
MyVariant Identifiers: chr9:g.25551126T>C (hg19) chr9:g.25551128T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551128T>C , CM000671.2:g.25551128T>C GRCh38
NC_000009.11:g.25551126T>C , CM000671.1:g.25551126T>C GRCh37
NC_000009.10:g.25541126T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-556A>G
XR_929525.2:n.674-556A>G
Search 100 bp 5'
Search 100 bp 3'