Canonical Allele Identifier: CA2612162293
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226975_5226978del , CM000673.2:g.5226975_5226978del GRCh38
NC_000011.9:g.5248205_5248208del , CM000673.1:g.5248205_5248208del GRCh37
NC_000011.8:g.5204781_5204784del NCBI36
NG_000007.3:g.70638_70641del
NG_059281.1:g.5094_5097del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.44_47del ENSP00000494175.1:p.Leu15ArgfsTer4
ENST00000335295.4:c.44_47del MANE Select ENSP00000333994.3:p.Leu15ArgfsTer4
ENST00000380315.2:c.44_47del ENSP00000369671.2:p.Leu15ArgfsTer4
ENST00000485743.1:n.95_98del
ENST00000633227.1:c.44_47del ENSP00000488004.1:p.Leu15ArgfsTer4
NM_000518.4:c.44_47del NP_000509.1:p.Leu15ArgfsTer4
NM_000518.5:c.44_47del MANE Select NP_000509.1:p.Leu15ArgfsTer4