Canonical Allele Identifier: CA2695213024
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225709del , CM000673.2:g.5225709del GRCh38
NC_000011.9:g.5246939del , CM000673.1:g.5246939del GRCh37
NC_000011.8:g.5203515del NCBI36
NG_000007.3:g.71908del
NG_059281.1:g.6364del

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.334del ENSP00000494175.1:p.Val112SerfsTer?
ENST00000335295.4:c.334del MANE Select ENSP00000333994.3:p.Val112SerfsTer?
ENST00000475226.1:n.266del
ENST00000633227.1:c.*150del ENSP00000488004.1:n.*150del
NM_000518.4:c.334del NP_000509.1:p.Val112SerfsTer?
NM_000518.5:c.334del MANE Select NP_000509.1:p.Val112SerfsTer?