Canonical Allele Identifier: CA2612162295
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227004_5227005insCT , CM000673.2:g.5227004_5227005insCT GRCh38
NC_000011.9:g.5248234_5248235insCT , CM000673.1:g.5248234_5248235insCT GRCh37
NC_000011.8:g.5204810_5204811insCT NCBI36
NG_000007.3:g.70611_70612insAG
NG_059281.1:g.5067_5068insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.17_18insAG ENSP00000494175.1:p.Glu7ValfsTer14
ENST00000335295.4:c.17_18insAG MANE Select ENSP00000333994.3:p.Glu7ValfsTer14
ENST00000380315.2:c.17_18insAG ENSP00000369671.2:p.Glu7ValfsTer14
ENST00000485743.1:n.68_69insAG
ENST00000633227.1:c.17_18insAG ENSP00000488004.1:p.Glu7ValfsTer14
NM_000518.4:c.17_18insAG NP_000509.1:p.Glu7ValfsTer14
NM_000518.5:c.17_18insAG MANE Select NP_000509.1:p.Glu7ValfsTer14