Canonical Allele Identifier: CA1949569835
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226827_5226831delinsCAGAG , CM000673.2:g.5226827_5226831delinsCAGAG GRCh38
NC_000011.9:g.5248057_5248061delinsCAGAG , CM000673.1:g.5248057_5248061delinsCAGAG GRCh37
NC_000011.8:g.5204633_5204637delinsCAGAG NCBI36
NG_000007.3:g.70785_70789delinsCTCTG
NG_059281.1:g.5241_5245delinsCTCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.93-32_93-28delinsCTCTG ENSP00000494175.1:n.93-32_93-28delinsCTCT...
ENST00000335295.4:c.93-32_93-28delinsCTCTG MANE Select ENSP00000333994.3:n.93-32_93-28delinsCTCT...
ENST00000380315.2:c.93-32_93-28delinsCTCTG ENSP00000369671.2:n.93-32_93-28delinsCTCT...
ENST00000485743.1:n.144-32_144-28delinsCTCTG
ENST00000633227.1:c.77-32_77-28delinsCTCTG ENSP00000488004.1:n.77-32_77-28delinsCTCT...
NM_000518.4:c.93-32_93-28delinsCTCTG NP_000509.1:n.93-32_93-28delinsCTCTG
NM_000518.5:c.93-32_93-28delinsCTCTG MANE Select NP_000509.1:n.93-32_93-28delinsCTCTG