Canonical Allele Identifier: CA1949567877
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226635_5226655delinsAAGGTGCCCTTGAGGTTGTCC , CM000673.2:g.5226635_5226655delinsAAGGTGCCCTTGAGGTTGTCC GRCh38
NC_000011.9:g.5247865_5247885delinsAAGGTGCCCTTGAGGTTGTCC , CM000673.1:g.5247865_5247885delinsAAGGTGCCCTTGAGGTTGTCC GRCh37
NC_000011.8:g.5204441_5204461delinsAAGGTGCCCTTGAGGTTGTCC NCBI36
NG_000007.3:g.70961_70981delinsGGACAACCTCAAGGGCACCTT
NG_059281.1:g.5417_5437delinsGGACAACCTCAAGGGCACCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.237_257delinsGGACAACCTCAAGGGCACCTT ENSP00000494175.1:p.Leu79=
ENST00000335295.4:c.237_257delinsGGACAACCTCAAGGGCACCTT MANE Select ENSP00000333994.3:p.Leu79=
ENST00000380315.2:c.237_257delinsGGACAACCTCAAGGGCACCTT ENSP00000369671.2:p.Leu79=
ENST00000475226.1:n.169_189delinsGGACAACCTCAAGGGCACCTT
ENST00000485743.1:n.288_308delinsGGACAACCTCAAGGGCACCTT
ENST00000633227.1:c.*53_*73delinsGGACAACCTCAAGGGCACCTT ENSP00000488004.1:n.*53_*73delinsGGACAACC...
NM_000518.4:c.237_257delinsGGACAACCTCAAGGGCACCTT NP_000509.1:p.Leu79=
NM_000518.5:c.237_257delinsGGACAACCTCAAGGGCACCTT MANE Select NP_000509.1:p.Leu79=