Canonical Allele Identifier: CA1949571454
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227056T= , CM000673.2:g.5227056T= GRCh38
NC_000011.9:g.5248286T= , CM000673.1:g.5248286T= GRCh37
NC_000011.8:g.5204862T= NCBI36
NG_000007.3:g.70560A=
NG_059281.1:g.5016A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-35A= ENSP00000494175.1:n.-35A=
ENST00000335295.4:c.-35A= MANE Select ENSP00000333994.3:n.-35A=
ENST00000380315.2:c.-18-17A= ENSP00000369671.2:n.-18-17A=
ENST00000485743.1:n.17A=
ENST00000633227.1:c.-35A= ENSP00000488004.1:n.-35A=
NM_000518.4:c.-35A= NP_000509.1:n.-35A=
NM_000518.5:c.-35A= MANE Select NP_000509.1:n.-35A=