Canonical Allele Identifier: CA677767929

Gene: HBG2

Linked Data

• dbSNP Id: rs35720845
• MyVariant Identifiers: chr11:g.5271309_5271310insGCTTA (hg19) ; chr11:g.5250079_5250080insGCTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5250079_5250080insGCTTA , CM000673.2:g.5250079_5250080insGCTTA	GRCh38
NC_000011.9:g.5271309_5271310insGCTTA , CM000673.1:g.5271309_5271310insGCTTA	GRCh37
NC_000011.8:g.5227885_5227886insGCTTA	NCBI36
NG_000007.3:g.47536_47537insTAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642908.1:c.316-1593_316-1592insTAAGC	ENSP00000495346.1:n.316-1593_316-1592insTAAGC
ENST00000647543.1:c.379-1593_379-1592insTAAGC	ENSP00000496470.1:n.379-1593_379-1592insTAAGC
ENST00000620888.4:c.316-1593_316-1592insTAAGC	ENSP00000479637.1:n.316-1593_316-1592insTAAGC