Canonical Allele Identifier: CA1949567685
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226617A= , CM000673.2:g.5226617A= GRCh38
NC_000011.9:g.5247847A= , CM000673.1:g.5247847A= GRCh37
NC_000011.8:g.5204423A= NCBI36
NG_000007.3:g.70999T=
NG_059281.1:g.5455T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.275T= ENSP00000494175.1:p.Leu92=
ENST00000335295.4:c.275T= MANE Select ENSP00000333994.3:p.Leu92=
ENST00000475226.1:n.207T=
ENST00000485743.1:n.326T=
ENST00000633227.1:c.*91T= ENSP00000488004.1:n.*91T=
NM_000518.4:c.275T= NP_000509.1:p.Leu92=
NM_000518.5:c.275T= MANE Select NP_000509.1:p.Leu92=