Canonical Allele Identifier: CA905231277
Gene:

Linked Data

dbSNP Id: rs957742274
gnomAD v3: 3-21207152-C-A
gnomAD v4: 3-21207152-C-A
MyVariant Identifiers: chr3:g.21248644C>A (hg19) chr3:g.21207152C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207152C>A , CM000665.2:g.21207152C>A GRCh38
NC_000003.11:g.21248644C>A , CM000665.1:g.21248644C>A GRCh37
NC_000003.10:g.21223648C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3846C>A
XR_940646.2:n.547-3846C>A
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