Canonical Allele Identifier: CA904086774
Gene:

Linked Data

dbSNP Id: rs1366510678
gnomAD v3: 3-187931605-C-G
gnomAD v4: 3-187931605-C-G
MyVariant Identifiers: chr3:g.187649393C>G (hg19) chr3:g.187931605C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931605C>G , CM000665.2:g.187931605C>G GRCh38
NC_000003.11:g.187649393C>G , CM000665.1:g.187649393C>G GRCh37
NC_000003.10:g.189132087C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1309G>C
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