Canonical Allele Identifier: CA2612162214
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225539del , CM000673.2:g.5225539del GRCh38
NC_000011.9:g.5246769del , CM000673.1:g.5246769del GRCh37
NC_000011.8:g.5203345del NCBI36
NG_000007.3:g.72077del
NG_059281.1:g.6533del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*59del ENSP00000494175.1:n.*59del
ENST00000335295.4:c.*59del MANE Select ENSP00000333994.3:n.*59del
ENST00000633227.1:c.*319del ENSP00000488004.1:n.*319del
NM_000518.4:c.*59del NP_000509.1:n.*59del
NM_000518.5:c.*59del MANE Select NP_000509.1:n.*59del