Canonical Allele Identifier: CA1949563792
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225507C= , CM000673.2:g.5225507C= GRCh38
NC_000011.9:g.5246737C= , CM000673.1:g.5246737C= GRCh37
NC_000011.8:g.5203313C= NCBI36
NG_000007.3:g.72109G=
NG_059281.1:g.6565G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*91G= ENSP00000494175.1:n.*91G=
ENST00000335295.4:c.*91G= MANE Select ENSP00000333994.3:n.*91G=
ENST00000633227.1:c.*351G= ENSP00000488004.1:n.*351G=
NM_000518.4:c.*91G= NP_000509.1:n.*91G=
NM_000518.5:c.*91G= MANE Select NP_000509.1:n.*91G=