Canonical Allele Identifier: CA1949568894
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226725_5226744delinsATAACAGCATCAGGAGTGGA , CM000673.2:g.5226725_5226744delinsATAACAGCATCAGGAGTGGA GRCh38
NC_000011.9:g.5247955_5247974delinsATAACAGCATCAGGAGTGGA , CM000673.1:g.5247955_5247974delinsATAACAGCATCAGGAGTGGA GRCh37
NC_000011.8:g.5204531_5204550delinsATAACAGCATCAGGAGTGGA NCBI36
NG_000007.3:g.70872_70891delinsTCCACTCCTGATGCTGTTAT
NG_059281.1:g.5328_5347delinsTCCACTCCTGATGCTGTTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.148_167delinsTCCACTCCTGATGCTGTTAT ENSP00000494175.1:p.Ser50=
ENST00000335295.4:c.148_167delinsTCCACTCCTGATGCTGTTAT MANE Select ENSP00000333994.3:p.Ser50=
ENST00000380315.2:c.148_167delinsTCCACTCCTGATGCTGTTAT ENSP00000369671.2:p.Ser50=
ENST00000475226.1:n.80_99delinsTCCACTCCTGATGCTGTTAT
ENST00000485743.1:n.199_218delinsTCCACTCCTGATGCTGTTAT
ENST00000633227.1:c.132_151delinsTCCACTCCTGATGCTGTTAT ENSP00000488004.1:p.Cys44=
NM_000518.4:c.148_167delinsTCCACTCCTGATGCTGTTAT NP_000509.1:p.Ser50=
NM_000518.5:c.148_167delinsTCCACTCCTGATGCTGTTAT MANE Select NP_000509.1:p.Ser50=