Canonical Allele Identifier: CA379264316

Gene: HBG2

Linked Data

• dbSNP Id: rs1228751398
• gnomAD v2: 11-5275615-A-G
• gnomAD v4: 11-5254385-A-G
• MyVariant Identifiers: chr11:g.5275615A>G (hg19) ; chr11:g.5254385A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254385A>G , CM000673.2:g.5254385A>G	GRCh38
NC_000011.9:g.5275615A>G , CM000673.1:g.5275615A>G	GRCh37
NC_000011.8:g.5232191A>G	NCBI36
NG_000007.3:g.43231T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336906.6:c.222T>C MANE Select	ENSP00000338082.4:p.Asp74=
ENST00000380252.6:c.57T>C	ENSP00000369602.2:p.Asp19=
ENST00000642908.1:c.222T>C	ENSP00000495346.1:p.Asp74=
ENST00000647543.1:c.222T>C	ENSP00000496470.1:p.Asp74=
ENST00000336906.4:c.222T>C	ENSP00000338082.4:p.Asp74=
ENST00000380252.5:c.192T>C	ENSP00000369602.1:p.Asp64=
ENST00000380259.6:c.222T>C	ENSP00000369609.2:p.Asp74=
ENST00000444587.1:c.*91T>C	ENSP00000488218.1:n.*91T>C
ENST00000620888.4:c.222T>C	ENSP00000479637.1:p.Asp74=
ENST00000624109.1:c.133A>G	ENSP00000485458.1:p.Ile45Val
NM_000184.2:c.222T>C	NP_000175.1:p.Asp74=
NM_000184.3:c.222T>C MANE Select	NP_000175.1:p.Asp74=