Canonical Allele Identifier: CA2574735556
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225531del , CM000673.2:g.5225531del GRCh38
NC_000011.9:g.5246761del , CM000673.1:g.5246761del GRCh37
NC_000011.8:g.5203337del NCBI36
NG_000007.3:g.72089del
NG_059281.1:g.6545del

Transcript Alleles

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