Canonical Allele Identifier: CA1949563830
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225527C= , CM000673.2:g.5225527C= GRCh38
NC_000011.9:g.5246757C= , CM000673.1:g.5246757C= GRCh37
NC_000011.8:g.5203333C= NCBI36
NG_000007.3:g.72089G=
NG_059281.1:g.6545G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*71G= ENSP00000494175.1:n.*71G=
ENST00000335295.4:c.*71G= MANE Select ENSP00000333994.3:n.*71G=
ENST00000633227.1:c.*331G= ENSP00000488004.1:n.*331G=
NM_000518.4:c.*71G= NP_000509.1:n.*71G=
NM_000518.5:c.*71G= MANE Select NP_000509.1:n.*71G=