Canonical Allele Identifier: CA1949567740
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226624_5226626delinsTCA , CM000673.2:g.5226624_5226626delinsTCA GRCh38
NC_000011.9:g.5247854_5247856delinsTCA , CM000673.1:g.5247854_5247856delinsTCA GRCh37
NC_000011.8:g.5204430_5204432delinsTCA NCBI36
NG_000007.3:g.70990_70992delinsTGA
NG_059281.1:g.5446_5448delinsTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.266_268delinsTGA ENSP00000494175.1:p.Leu89=
ENST00000335295.4:c.266_268delinsTGA MANE Select ENSP00000333994.3:p.Leu89=
ENST00000380315.2:c.266_268delinsTGA ENSP00000369671.2:p.Leu89=
ENST00000475226.1:n.198_200delinsTGA
ENST00000485743.1:n.317_319delinsTGA
ENST00000633227.1:c.*82_*84delinsTGA ENSP00000488004.1:n.*82_*84delinsTGA
NM_000518.4:c.266_268delinsTGA NP_000509.1:p.Leu89=
NM_000518.5:c.266_268delinsTGA MANE Select NP_000509.1:p.Leu89=