Canonical Allele Identifier: CA200491788
Gene:

Linked Data

dbSNP Id: rs367681418
gnomAD v3: 9-129576953-T-C
gnomAD v4: 9-129576953-T-C
MyVariant Identifiers: chr9:g.132339232T>C (hg19) chr9:g.129576953T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576953T>C , CM000671.2:g.129576953T>C GRCh38
NC_000009.11:g.132339232T>C , CM000671.1:g.132339232T>C GRCh37
NC_000009.10:g.131379053T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1355T>C
Search 100 bp 5'
Search 100 bp 3'