Canonical Allele Identifier: CA200491738
Gene:

Linked Data

dbSNP Id: rs573378130
gnomAD v2: 9-132339185-T-A
gnomAD v3: 9-129576906-T-A
gnomAD v4: 9-129576906-T-A
MyVariant Identifiers: chr9:g.132339185T>A (hg19) chr9:g.129576906T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576906T>A , CM000671.2:g.129576906T>A GRCh38
NC_000009.11:g.132339185T>A , CM000671.1:g.132339185T>A GRCh37
NC_000009.10:g.131379006T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1308T>A
Search 100 bp 5'
Search 100 bp 3'