Canonical Allele Identifier: CA1282456532
Gene:

Linked Data

dbSNP Id: rs1678010248
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079875_118079876insCTTGTT , CM000664.2:g.118079875_118079876insCTTGTT GRCh38
NC_000002.11:g.118837451_118837452insCTTGTT , CM000664.1:g.118837451_118837452insCTTGTT GRCh37
NC_000002.10:g.118553921_118553922insCTTGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2344_697-2343insAACAAG XP_011510607.1:n.697-2344_697-2343insAACAAG
XR_001739662.2:n.138+8375_138+8376insAACAAG
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