Canonical Allele Identifier: CA2612162118

Gene: HBB

Linked Data

• gnomAD v4: 11-5226429-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226433del , CM000673.2:g.5226433del	GRCh38
NC_000011.9:g.5247663del , CM000673.1:g.5247663del	GRCh37
NC_000011.8:g.5204239del	NCBI36
NG_000007.3:g.71186del
NG_059281.1:g.5642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.315+147del	ENSP00000494175.1:n.315+147del
ENST00000335295.4:c.315+147del MANE Select	ENSP00000333994.3:n.315+147del
ENST00000475226.1:n.247+147del
ENST00000485743.1:n.513del
ENST00000633227.1:c.*131+147del	ENSP00000488004.1:n.*131+147del
NM_000518.4:c.315+147del	NP_000509.1:n.315+147del
NM_000518.5:c.315+147del MANE Select	NP_000509.1:n.315+147del