Canonical Allele Identifier: CA55082011
Gene:

Linked Data

dbSNP Id: rs765002229
MyVariant Identifiers: chr2:g.123641459C>A (hg19) chr2:g.122883883C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883883C>A , CM000664.2:g.122883883C>A GRCh38
NC_000002.11:g.123641459C>A , CM000664.1:g.123641459C>A GRCh37
NC_000002.10:g.123357929C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1059C>A
XR_001739692.1:n.1451-1059C>A
XR_923292.2:n.1358-1059C>A
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