Canonical Allele Identifier: CA1949563801
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225513G= , CM000673.2:g.5225513G= GRCh38
NC_000011.9:g.5246743G= , CM000673.1:g.5246743G= GRCh37
NC_000011.8:g.5203319G= NCBI36
NG_000007.3:g.72103C=
NG_059281.1:g.6559C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*85C= ENSP00000494175.1:n.*85C=
ENST00000335295.4:c.*85C= MANE Select ENSP00000333994.3:n.*85C=
ENST00000633227.1:c.*345C= ENSP00000488004.1:n.*345C=
NM_000518.4:c.*85C= NP_000509.1:n.*85C=
NM_000518.5:c.*85C= MANE Select NP_000509.1:n.*85C=