Canonical Allele Identifier: CA1949564691
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225659_5225665delinsTGCACTG , CM000673.2:g.5225659_5225665delinsTGCACTG GRCh38
NC_000011.9:g.5246889_5246895delinsTGCACTG , CM000673.1:g.5246889_5246895delinsTGCACTG GRCh37
NC_000011.8:g.5203465_5203471delinsTGCACTG NCBI36
NG_000007.3:g.71951_71957delinsCAGTGCA
NG_059281.1:g.6407_6413delinsCAGTGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.377_383delinsCAGTGCA ENSP00000494175.1:p.Pro126=
ENST00000335295.4:c.377_383delinsCAGTGCA MANE Select ENSP00000333994.3:p.Pro126=
ENST00000475226.1:n.309_315delinsCAGTGCA
ENST00000633227.1:c.*193_*199delinsCAGTGCA ENSP00000488004.1:n.*193_*199delinsCAGTGC...
NM_000518.4:c.377_383delinsCAGTGCA NP_000509.1:p.Pro126=
NM_000518.5:c.377_383delinsCAGTGCA MANE Select NP_000509.1:p.Pro126=