Canonical Allele Identifier: CA934695822

Gene: HBG2

Linked Data

• gnomAD v3: 11-5250078-C-CTGAT
• gnomAD v4: 11-5250078-C-CTGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5250079_5250080insGATT , CM000673.2:g.5250079_5250080insGATT	GRCh38
NC_000011.9:g.5271309_5271310insGATT , CM000673.1:g.5271309_5271310insGATT	GRCh37
NC_000011.8:g.5227885_5227886insGATT	NCBI36
NG_000007.3:g.47537_47538insATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642908.1:c.316-1592_316-1591insATCA	ENSP00000495346.1:n.316-1592_316-1591insATCA
ENST00000647543.1:c.379-1592_379-1591insATCA	ENSP00000496470.1:n.379-1592_379-1591insATCA
ENST00000620888.4:c.316-1592_316-1591insATCA	ENSP00000479637.1:n.316-1592_316-1591insATCA