Canonical Allele Identifier: CA597436182

Gene: HBG1 HBG2

Linked Data

• dbSNP Id: rs1455757089
• gnomAD v2: 11-5270921-T-A
• gnomAD v4: 11-5249691-T-A
• MyVariant Identifiers: chr11:g.5270921T>A (hg19) ; chr11:g.5249691T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249691T>A , CM000673.2:g.5249691T>A	GRCh38
NC_000011.9:g.5270921T>A , CM000673.1:g.5270921T>A	GRCh37
NC_000011.8:g.5227497T>A	NCBI36
NG_000007.3:g.47925A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.92+22A>T (HBG1) MANE Select	ENSP00000327431.4:n.92+22A>T
ENST00000642908.1:c.316-1204A>T	ENSP00000495346.1:n.316-1204A>T
ENST00000647543.1:c.379-1204A>T	ENSP00000496470.1:n.379-1204A>T
ENST00000648735.1:n.143+22A>T (HBG1)
ENST00000330597.3:c.92+22A>T (HBG1)	ENSP00000327431.3:n.92+22A>T
ENST00000620888.4:c.316-1204A>T (HBG2)	ENSP00000479637.1:n.316-1204A>T
ENST00000623781.1:c.265-21T>A	ENSP00000485381.1:n.265-21T>A
ENST00000632727.1:c.54+60A>T (HBG1)	ENSP00000488759.1:n.54+60A>T
NM_000559.2:c.92+22A>T (HBG1)	NP_000550.2:n.92+22A>T
NM_000559.3:c.92+22A>T (HBG1) MANE Select	NP_000550.2:n.92+22A>T