Canonical Allele Identifier: CA589717557
Gene:

Linked Data

dbSNP Id: rs1327461243
gnomAD v2: 9-110855089-G-C
gnomAD v3: 9-108092808-G-C
gnomAD v4: 9-108092808-G-C
MyVariant Identifiers: chr9:g.110855089G>C (hg19) chr9:g.108092808G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092808G>C , CM000671.2:g.108092808G>C GRCh38
NC_000009.11:g.110855089G>C , CM000671.1:g.110855089G>C GRCh37
NC_000009.10:g.109894910G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39514C>G
XR_001746881.1:n.668-39514C>G
XR_001746882.1:n.668-39514C>G
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