Canonical Allele Identifier: CA597436185

Gene: HBG1 HBG2

Linked Data

• dbSNP Id: rs1399955620
• gnomAD v2: 11-5270948-CA-C
• gnomAD v4: 11-5249718-CA-C
• MyVariant Identifiers: chr11:g.5270949del (hg19) ; chr11:g.5249719del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249719del , CM000673.2:g.5249719del	GRCh38
NC_000011.9:g.5270949del , CM000673.1:g.5270949del	GRCh37
NC_000011.8:g.5227525del	NCBI36
NG_000007.3:g.47897del

Transcript Alleles

HGVS	Amino-acid change
ENST00000330597.5:c.86del (HBG1) MANE Select	ENSP00000327431.4:p.Leu29ArgfsTer?
ENST00000642908.1:c.316-1232del	ENSP00000495346.1:n.316-1232del
ENST00000647543.1:c.379-1232del	ENSP00000496470.1:n.379-1232del
ENST00000648735.1:n.137del (HBG1)
ENST00000330597.3:c.86del (HBG1)	ENSP00000327431.3:p.Leu29ArgfsTer?
ENST00000620888.4:c.316-1232del (HBG2)	ENSP00000479637.1:n.316-1232del
ENST00000623781.1:c.272del	ENSP00000485381.1:p.Gln91ArgfsTer27
ENST00000632727.1:c.54+32del (HBG1)	ENSP00000488759.1:n.54+32del
NM_000559.2:c.86del (HBG1)	NP_000550.2:p.Leu29ArgfsTer?
NM_000559.3:c.86del (HBG1) MANE Select	NP_000550.2:p.Leu29ArgfsTer?