Canonical Allele Identifier: CA379280259

Gene: HBG1 HBG2

Linked Data

• gnomAD v4: 11-5249572-T-G
• MyVariant Identifiers: chr11:g.5270802T>G (hg19) ; chr11:g.5249572T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249572T>G , CM000673.2:g.5249572T>G	GRCh38
NC_000011.9:g.5270802T>G , CM000673.1:g.5270802T>G	GRCh37
NC_000011.8:g.5227378T>G	NCBI36
NG_000007.3:g.48044A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.111A>C (HBG1) MANE Select	ENSP00000327431.4:p.Pro37=
ENST00000642908.1:c.316-1085A>C	ENSP00000495346.1:n.316-1085A>C
ENST00000647543.1:c.379-1085A>C	ENSP00000496470.1:n.379-1085A>C
ENST00000648735.1:n.162A>C (HBG1)
ENST00000330597.3:c.111A>C (HBG1)	ENSP00000327431.3:p.Pro37=
ENST00000620888.4:c.316-1085A>C (HBG2)	ENSP00000479637.1:n.316-1085A>C
ENST00000623781.1:c.244T>G	ENSP00000485381.1:p.Trp82Gly
ENST00000632727.1:c.73A>C (HBG1)	ENSP00000488759.1:p.Met25Leu
NM_000559.2:c.111A>C (HBG1)	NP_000550.2:p.Pro37=
NM_000559.3:c.111A>C (HBG1) MANE Select	NP_000550.2:p.Pro37=