Canonical Allele Identifier: CA1284674299
Gene:

Linked Data

dbSNP Id: rs1573479121
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884138G>A , CM000664.2:g.122884138G>A GRCh38
NC_000002.11:g.123641714G>A , CM000664.1:g.123641714G>A GRCh37
NC_000002.10:g.123358184G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-804G>A
XR_001739692.1:n.1451-804G>A
XR_923292.2:n.1358-804G>A
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