Canonical Allele Identifier: CA1481406928

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102500941_102500943delinsACT , CM000666.2:g.102500941_102500943delinsACT	GRCh38
NC_000004.11:g.103422098_103422100delinsACT , CM000666.1:g.103422098_103422100delinsACT	GRCh37
NC_000004.10:g.103641130_103641132delinsACT	NCBI36
NG_050628.1:g.4613_4615delinsACT

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+306_643+308delinsAGT	XP_011530769.1:n.643+306_643+308delinsAGT
NR_136202.1:n.48+1496_48+1498delinsAGT