Canonical Allele Identifier: CA1949567195
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226563T= , CM000673.2:g.5226563T= GRCh38
NC_000011.9:g.5247793T= , CM000673.1:g.5247793T= GRCh37
NC_000011.8:g.5204369T= NCBI36
NG_000007.3:g.71053A=
NG_059281.1:g.5509A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+14A= ENSP00000494175.1:n.315+14A=
ENST00000335295.4:c.315+14A= MANE Select ENSP00000333994.3:n.315+14A=
ENST00000475226.1:n.247+14A=
ENST00000485743.1:n.380A=
ENST00000633227.1:c.*131+14A= ENSP00000488004.1:n.*131+14A=
NM_000518.4:c.315+14A= NP_000509.1:n.315+14A=
NM_000518.5:c.315+14A= MANE Select NP_000509.1:n.315+14A=