Canonical Allele Identifier: CA2612162247
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225578del , CM000673.2:g.5225578del GRCh38
NC_000011.9:g.5246808del , CM000673.1:g.5246808del GRCh37
NC_000011.8:g.5203384del NCBI36
NG_000007.3:g.72039del
NG_059281.1:g.6495del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*21del ENSP00000494175.1:n.*21del
ENST00000335295.4:c.*21del MANE Select ENSP00000333994.3:n.*21del
ENST00000633227.1:c.*281del ENSP00000488004.1:n.*281del
NM_000518.4:c.*21del NP_000509.1:n.*21del
NM_000518.5:c.*21del MANE Select NP_000509.1:n.*21del