Canonical Allele Identifier: CA1332325162
Gene:

Linked Data

dbSNP Id: rs1691990726
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.226155958G>A , CM000664.2:g.226155958G>A GRCh38
NC_000002.11:g.227020674G>A , CM000664.1:g.227020674G>A GRCh37
NC_000002.10:g.226728918G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046102.1:n.293-8430G>A
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