Canonical Allele Identifier: CA1949567042
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226487_5226489delinsCTG , CM000673.2:g.5226487_5226489delinsCTG GRCh38
NC_000011.9:g.5247717_5247719delinsCTG , CM000673.1:g.5247717_5247719delinsCTG GRCh37
NC_000011.8:g.5204293_5204295delinsCTG NCBI36
NG_000007.3:g.71127_71129delinsCAG
NG_059281.1:g.5583_5585delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+88_315+90delinsCAG ENSP00000494175.1:n.315+88_315+90delinsCA...
ENST00000335295.4:c.315+88_315+90delinsCAG MANE Select ENSP00000333994.3:n.315+88_315+90delinsCA...
ENST00000475226.1:n.247+88_247+90delinsCAG
ENST00000485743.1:n.454_456delinsCAG
ENST00000633227.1:c.*131+88_*131+90delinsCAG ENSP00000488004.1:n.*131+88_*131+90delins...
NM_000518.4:c.315+88_315+90delinsCAG NP_000509.1:n.315+88_315+90delinsCAG
NM_000518.5:c.315+88_315+90delinsCAG MANE Select NP_000509.1:n.315+88_315+90delinsCAG