Canonical Allele Identifier: CA55082073
Gene:

Linked Data

dbSNP Id: rs1009269799
gnomAD v2: 2-123641731-T-A
gnomAD v3: 2-122884155-T-A
gnomAD v4: 2-122884155-T-A
MyVariant Identifiers: chr2:g.123641731T>A (hg19) chr2:g.122884155T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884155T>A , CM000664.2:g.122884155T>A GRCh38
NC_000002.11:g.123641731T>A , CM000664.1:g.123641731T>A GRCh37
NC_000002.10:g.123358201T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-787T>A
XR_001739692.1:n.1451-787T>A
XR_923292.2:n.1358-787T>A
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