Canonical Allele Identifier: CA1949565114
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225704_5225716delinsCAGACCAGCACGT , CM000673.2:g.5225704_5225716delinsCAGACCAGCACGT GRCh38
NC_000011.9:g.5246934_5246946delinsCAGACCAGCACGT , CM000673.1:g.5246934_5246946delinsCAGACCAGCACGT GRCh37
NC_000011.8:g.5203510_5203522delinsCAGACCAGCACGT NCBI36
NG_000007.3:g.71900_71912delinsACGTGCTGGTCTG
NG_059281.1:g.6356_6368delinsACGTGCTGGTCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.326_338delinsACGTGCTGGTCTG ENSP00000494175.1:p.Asn109=
ENST00000335295.4:c.326_338delinsACGTGCTGGTCTG MANE Select ENSP00000333994.3:p.Asn109=
ENST00000475226.1:n.258_270delinsACGTGCTGGTCTG
ENST00000633227.1:c.*142_*154delinsACGTGCTGGTCTG ENSP00000488004.1:n.*142_*154delinsACGTGC...
NM_000518.4:c.326_338delinsACGTGCTGGTCTG NP_000509.1:p.Asn109=
NM_000518.5:c.326_338delinsACGTGCTGGTCTG MANE Select NP_000509.1:p.Asn109=