Canonical Allele Identifier: CA1949569840
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226830A= , CM000673.2:g.5226830A= GRCh38
NC_000011.9:g.5248060A= , CM000673.1:g.5248060A= GRCh37
NC_000011.8:g.5204636A= NCBI36
NG_000007.3:g.70786T=
NG_059281.1:g.5242T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.93-31T= ENSP00000494175.1:n.93-31T=
ENST00000335295.4:c.93-31T= MANE Select ENSP00000333994.3:n.93-31T=
ENST00000380315.2:c.93-31T= ENSP00000369671.2:n.93-31T=
ENST00000485743.1:n.144-31T=
ENST00000633227.1:c.77-31T= ENSP00000488004.1:n.77-31T=
NM_000518.4:c.93-31T= NP_000509.1:n.93-31T=
NM_000518.5:c.93-31T= MANE Select NP_000509.1:n.93-31T=