Canonical Allele Identifier: CA1949570595
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226962_5226968delinsGTTCACC , CM000673.2:g.5226962_5226968delinsGTTCACC GRCh38
NC_000011.9:g.5248192_5248198delinsGTTCACC , CM000673.1:g.5248192_5248198delinsGTTCACC GRCh37
NC_000011.8:g.5204768_5204774delinsGTTCACC NCBI36
NG_000007.3:g.70648_70654delinsGGTGAAC
NG_059281.1:g.5104_5110delinsGGTGAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.54_60delinsGGTGAAC ENSP00000494175.1:p.Lys18=
ENST00000335295.4:c.54_60delinsGGTGAAC MANE Select ENSP00000333994.3:p.Lys18=
ENST00000380315.2:c.54_60delinsGGTGAAC ENSP00000369671.2:p.Lys18=
ENST00000485743.1:n.105_111delinsGGTGAAC
ENST00000633227.1:c.54_60delinsGGTGAAC ENSP00000488004.1:p.Lys18=
NM_000518.4:c.54_60delinsGGTGAAC NP_000509.1:p.Lys18=
NM_000518.5:c.54_60delinsGGTGAAC MANE Select NP_000509.1:p.Lys18=