Canonical Allele Identifier: CA1949568962
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226734T= , CM000673.2:g.5226734T= GRCh38
NC_000011.9:g.5247964T= , CM000673.1:g.5247964T= GRCh37
NC_000011.8:g.5204540T= NCBI36
NG_000007.3:g.70882A=
NG_059281.1:g.5338A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.158A= ENSP00000494175.1:p.Asp53=
ENST00000335295.4:c.158A= MANE Select ENSP00000333994.3:p.Asp53=
ENST00000380315.2:c.158A= ENSP00000369671.2:p.Asp53=
ENST00000475226.1:n.90A=
ENST00000485743.1:n.209A=
ENST00000633227.1:c.142A= ENSP00000488004.1:p.Met48=
NM_000518.4:c.158A= NP_000509.1:p.Asp53=
NM_000518.5:c.158A= MANE Select NP_000509.1:p.Asp53=