Canonical Allele Identifier: CA1949569523
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226780A= , CM000673.2:g.5226780A= GRCh38
NC_000011.9:g.5248010A= , CM000673.1:g.5248010A= GRCh37
NC_000011.8:g.5204586A= NCBI36
NG_000007.3:g.70836T=
NG_059281.1:g.5292T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.112T= ENSP00000494175.1:p.Trp38=
ENST00000335295.4:c.112T= MANE Select ENSP00000333994.3:p.Trp38=
ENST00000380315.2:c.112T= ENSP00000369671.2:p.Trp38=
ENST00000475226.1:n.44T=
ENST00000485743.1:n.163T=
ENST00000633227.1:c.96T= ENSP00000488004.1:p.Leu32=
NM_000518.4:c.112T= NP_000509.1:p.Trp38=
NM_000518.5:c.112T= MANE Select NP_000509.1:p.Trp38=