Canonical Allele Identifier: CA379280095

Gene: HBG1 HBG2

Linked Data

• gnomAD v4: 11-5249514-C-A
• MyVariant Identifiers: chr11:g.5270744C>A (hg19) ; chr11:g.5249514C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249514C>A , CM000673.2:g.5249514C>A	GRCh38
NC_000011.9:g.5270744C>A , CM000673.1:g.5270744C>A	GRCh37
NC_000011.8:g.5227320C>A	NCBI36
NG_000007.3:g.48102G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.169G>T (HBG1) MANE Select	ENSP00000327431.4:p.Gly57Cys
ENST00000642908.1:c.316-1027G>T	ENSP00000495346.1:n.316-1027G>T
ENST00000647543.1:c.379-1027G>T	ENSP00000496470.1:n.379-1027G>T
ENST00000648735.1:n.220G>T (HBG1)
ENST00000330597.3:c.169G>T (HBG1)	ENSP00000327431.3:p.Gly57Cys
ENST00000620888.4:c.316-1027G>T (HBG2)	ENSP00000479637.1:n.316-1027G>T
ENST00000623781.1:c.186C>A	ENSP00000485381.1:p.Ala62=
ENST00000632727.1:c.*38G>T (HBG1)	ENSP00000488759.1:n.*38G>T
NM_000559.2:c.169G>T (HBG1)	NP_000550.2:p.Gly57Cys
NM_000559.3:c.169G>T (HBG1) MANE Select	NP_000550.2:p.Gly57Cys