Canonical Allele Identifier: CA198558669
Gene:

Linked Data

dbSNP Id: rs10980800
gnomAD v2: 9-113915905-T-C
gnomAD v3: 9-111153625-T-C
gnomAD v4: 9-111153625-T-C
MyVariant Identifiers: chr9:g.113915905T>C (hg19) chr9:g.111153625T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111153625T>C , CM000671.2:g.111153625T>C GRCh38
NC_000009.11:g.113915905T>C , CM000671.1:g.113915905T>C GRCh37
NC_000009.10:g.112955726T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930247.1:n.477-14006A>G
XR_930248.1:n.557-14006A>G
XR_930249.1:n.477-14006A>G
XR_001746893.1:n.477-14006A>G
XR_001746894.1:n.477-14006A>G
XR_930247.2:n.477-14006A>G
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