Canonical Allele Identifier: CA379279931

Gene: HBG1 HBG2

Linked Data

• dbSNP Id: rs1061234
• gnomAD v3: 11-5249456-G-C
• gnomAD v4: 11-5249456-G-C
• MyVariant Identifiers: chr11:g.5270686G>C (hg19) ; chr11:g.5249456G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249456G>C , CM000673.2:g.5249456G>C	GRCh38
NC_000011.9:g.5270686G>C , CM000673.1:g.5270686G>C	GRCh37
NC_000011.8:g.5227262G>C	NCBI36
NG_000007.3:g.48160C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.227C>G (HBG1) MANE Select	ENSP00000327431.4:p.Thr76Arg
ENST00000642908.1:c.316-969C>G	ENSP00000495346.1:n.316-969C>G
ENST00000647543.1:c.379-969C>G	ENSP00000496470.1:n.379-969C>G
ENST00000648735.1:n.278C>G (HBG1)
ENST00000330597.3:c.227C>G (HBG1)	ENSP00000327431.3:p.Thr76Arg
ENST00000620888.4:c.316-969C>G (HBG2)	ENSP00000479637.1:n.316-969C>G
ENST00000623781.1:c.128G>C	ENSP00000485381.1:p.Cys43Ser
ENST00000632727.1:c.*96C>G (HBG1)	ENSP00000488759.1:n.*96C>G
NM_000559.2:c.227C>G (HBG1)	NP_000550.2:p.Thr76Arg
NM_000559.3:c.227C>G (HBG1) MANE Select	NP_000550.2:p.Thr76Arg