Canonical Allele Identifier: CA5840275

Gene: HBG2

Linked Data

• dbSNP Id: rs756203751
• ExAC: 11:5275726 T / C
• gnomAD v2: 11-5275726-T-C
• gnomAD v4: 11-5254496-T-C
• MyVariant Identifiers: chr11:g.5275726T>C (hg19) ; chr11:g.5254496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254496T>C , CM000673.2:g.5254496T>C	GRCh38
NC_000011.9:g.5275726T>C , CM000673.1:g.5275726T>C	GRCh37
NC_000011.8:g.5232302T>C	NCBI36
NG_000007.3:g.43120A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.111A>G MANE Select	ENSP00000338082.4:p.Pro37=
ENST00000380252.6:c.-55A>G	ENSP00000369602.2:n.-55A>G
ENST00000380259.7:c.1657A>G	ENSP00000369609.3:n.1657A>G
ENST00000642908.1:c.111A>G	ENSP00000495346.1:p.Pro37=
ENST00000647543.1:c.111A>G	ENSP00000496470.1:p.Pro37=
ENST00000336906.4:c.111A>G	ENSP00000338082.4:p.Pro37=
ENST00000380252.5:c.81A>G	ENSP00000369602.1:p.Pro27=
ENST00000380259.6:c.111A>G	ENSP00000369609.2:p.Pro37=
ENST00000444587.1:c.73A>G	ENSP00000488218.1:p.Met25Val
ENST00000620888.4:c.111A>G	ENSP00000479637.1:p.Pro37=
ENST00000624109.1:c.244T>C	ENSP00000485458.1:p.Trp82Arg
NM_000184.2:c.111A>G	NP_000175.1:p.Pro37=
NM_000184.3:c.111A>G MANE Select	NP_000175.1:p.Pro37=