Canonical Allele Identifier: CA1284674009
Gene:

Linked Data

dbSNP Id: rs1680370978
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883825G>A , CM000664.2:g.122883825G>A GRCh38
NC_000002.11:g.123641401G>A , CM000664.1:g.123641401G>A GRCh37
NC_000002.10:g.123357871G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1117G>A
XR_001739692.1:n.1451-1117G>A
XR_923292.2:n.1358-1117G>A
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