Canonical Allele Identifier: CA1300258629

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870211_155870212delinsAT , CM000664.2:g.155870211_155870212delinsAT	GRCh38
NC_000002.11:g.156726723_156726724delinsAT , CM000664.1:g.156726723_156726724delinsAT	GRCh37
NC_000002.10:g.156434969_156434970delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3025_320-3024delinsAT
XR_001739749.1:n.331-29228_331-29227delinsAT
XR_001739750.1:n.331-29228_331-29227delinsAT
XR_001739751.1:n.331-29228_331-29227delinsAT
XR_923501.2:n.331-3025_331-3024delinsAT