Canonical Allele Identifier: CA1949563839
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225531C= , CM000673.2:g.5225531C= GRCh38
NC_000011.9:g.5246761C= , CM000673.1:g.5246761C= GRCh37
NC_000011.8:g.5203337C= NCBI36
NG_000007.3:g.72085G=
NG_059281.1:g.6541G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*67G= ENSP00000494175.1:n.*67G=
ENST00000335295.4:c.*67G= MANE Select ENSP00000333994.3:n.*67G=
ENST00000633227.1:c.*327G= ENSP00000488004.1:n.*327G=
NM_000518.4:c.*67G= NP_000509.1:n.*67G=
NM_000518.5:c.*67G= MANE Select NP_000509.1:n.*67G=