Canonical Allele Identifier: CA1949567184
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226562G= , CM000673.2:g.5226562G= GRCh38
NC_000011.9:g.5247792G= , CM000673.1:g.5247792G= GRCh37
NC_000011.8:g.5204368G= NCBI36
NG_000007.3:g.71054C=
NG_059281.1:g.5510C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+15C= ENSP00000494175.1:n.315+15C=
ENST00000335295.4:c.315+15C= MANE Select ENSP00000333994.3:n.315+15C=
ENST00000475226.1:n.247+15C=
ENST00000485743.1:n.381C=
ENST00000633227.1:c.*131+15C= ENSP00000488004.1:n.*131+15C=
NM_000518.4:c.315+15C= NP_000509.1:n.315+15C=
NM_000518.5:c.315+15C= MANE Select NP_000509.1:n.315+15C=