Canonical Allele Identifier: CA1949563814
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225520A= , CM000673.2:g.5225520A= GRCh38
NC_000011.9:g.5246750A= , CM000673.1:g.5246750A= GRCh37
NC_000011.8:g.5203326A= NCBI36
NG_000007.3:g.72096T=
NG_059281.1:g.6552T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*78T= ENSP00000494175.1:n.*78T=
ENST00000335295.4:c.*78T= MANE Select ENSP00000333994.3:n.*78T=
ENST00000633227.1:c.*338T= ENSP00000488004.1:n.*338T=
NM_000518.4:c.*78T= NP_000509.1:n.*78T=
NM_000518.5:c.*78T= MANE Select NP_000509.1:n.*78T=