Canonical Allele Identifier: CA379280222

Gene: HBG1 HBG2

Linked Data

• MyVariant Identifiers: chr11:g.5270788A>G (hg19) ; chr11:g.5249558A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249558A>G , CM000673.2:g.5249558A>G	GRCh38
NC_000011.9:g.5270788A>G , CM000673.1:g.5270788A>G	GRCh37
NC_000011.8:g.5227364A>G	NCBI36
NG_000007.3:g.48058T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.125T>C (HBG1) MANE Select	ENSP00000327431.4:p.Phe42Ser
ENST00000642908.1:c.316-1071T>C	ENSP00000495346.1:n.316-1071T>C
ENST00000647543.1:c.379-1071T>C	ENSP00000496470.1:n.379-1071T>C
ENST00000648735.1:n.176T>C (HBG1)
ENST00000330597.3:c.125T>C (HBG1)	ENSP00000327431.3:p.Phe42Ser
ENST00000620888.4:c.316-1071T>C (HBG2)	ENSP00000479637.1:n.316-1071T>C
ENST00000623781.1:c.230A>G	ENSP00000485381.1:p.Glu77Gly
ENST00000632727.1:c.87T>C (HBG1)	ENSP00000488759.1:p.Val29=
NM_000559.2:c.125T>C (HBG1)	NP_000550.2:p.Phe42Ser
NM_000559.3:c.125T>C (HBG1) MANE Select	NP_000550.2:p.Phe42Ser