Canonical Allele Identifier: CA1481405950
Gene:

Linked Data

dbSNP Id: rs1738897344
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500030C>T , CM000666.2:g.102500030C>T GRCh38
NC_000004.11:g.103421187C>T , CM000666.1:g.103421187C>T GRCh37
NC_000004.10:g.103640219C>T NCBI36
NG_050628.1:g.3702C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1219G>A XP_011530769.1:n.643+1219G>A
NR_136202.1:n.48+2409G>A
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