Canonical Allele Identifier: CA1949565716
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225828_5225839delinsGGTAGCTGGATT , CM000673.2:g.5225828_5225839delinsGGTAGCTGGATT GRCh38
NC_000011.9:g.5247058_5247069delinsGGTAGCTGGATT , CM000673.1:g.5247058_5247069delinsGGTAGCTGGATT GRCh37
NC_000011.8:g.5203634_5203645delinsGGTAGCTGGATT NCBI36
NG_000007.3:g.71777_71788delinsAATCCAGCTACC
NG_059281.1:g.6233_6244delinsAATCCAGCTACC

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316-113_316-102delinsAATCCAGCTACC ENSP00000494175.1:n.316-113_316-102delins...
ENST00000335295.4:c.316-113_316-102delinsAATCCAGCTACC MANE Select ENSP00000333994.3:n.316-113_316-102delins...
ENST00000475226.1:n.248-113_248-102delinsAATCCAGCTACC
ENST00000633227.1:c.*132-113_*132-102delinsAATCCAGCTACC ENSP00000488004.1:n.*132-113_*132-102deli...
NM_000518.4:c.316-113_316-102delinsAATCCAGCTACC NP_000509.1:n.316-113_316-102delinsAATCCA...
NM_000518.5:c.316-113_316-102delinsAATCCAGCTACC MANE Select NP_000509.1:n.316-113_316-102delinsAATCCA...