Canonical Allele Identifier: CA13019018
Gene:

Linked Data

dbSNP Id: rs12006166
gnomAD v2: 9-118424987-A-T
gnomAD v3: 9-115662708-A-T
gnomAD v4: 9-115662708-A-T
MyVariant Identifiers: chr9:g.118424987A>T (hg19) chr9:g.115662708A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115662708A>T , CM000671.2:g.115662708A>T GRCh38
NC_000009.11:g.118424987A>T , CM000671.1:g.118424987A>T GRCh37
NC_000009.10:g.117464808A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930270.1:n.170-1676A>T
XR_930270.2:n.353-1676A>T
Search 100 bp 5'
Search 100 bp 3'