Canonical Allele Identifier: CA1949568940
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226732C= , CM000673.2:g.5226732C= GRCh38
NC_000011.9:g.5247962C= , CM000673.1:g.5247962C= GRCh37
NC_000011.8:g.5204538C= NCBI36
NG_000007.3:g.70884G=
NG_059281.1:g.5340G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.160G= ENSP00000494175.1:p.Ala54=
ENST00000335295.4:c.160G= MANE Select ENSP00000333994.3:p.Ala54=
ENST00000380315.2:c.160G= ENSP00000369671.2:p.Ala54=
ENST00000475226.1:n.92G=
ENST00000485743.1:n.211G=
ENST00000633227.1:c.144G= ENSP00000488004.1:p.Met48=
NM_000518.4:c.160G= NP_000509.1:p.Ala54=
NM_000518.5:c.160G= MANE Select NP_000509.1:p.Ala54=