Canonical Allele Identifier: CA1949567949
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226640_5226641delinsGC , CM000673.2:g.5226640_5226641delinsGC GRCh38
NC_000011.9:g.5247870_5247871delinsGC , CM000673.1:g.5247870_5247871delinsGC GRCh37
NC_000011.8:g.5204446_5204447delinsGC NCBI36
NG_000007.3:g.70975_70976delinsGC
NG_059281.1:g.5431_5432delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.251_252delinsGC ENSP00000494175.1:p.Gly84=
ENST00000335295.4:c.251_252delinsGC MANE Select ENSP00000333994.3:p.Gly84=
ENST00000380315.2:c.251_252delinsGC ENSP00000369671.2:p.Gly84=
ENST00000475226.1:n.183_184delinsGC
ENST00000485743.1:n.302_303delinsGC
ENST00000633227.1:c.*67_*68delinsGC ENSP00000488004.1:n.*67_*68delinsGC
NM_000518.4:c.251_252delinsGC NP_000509.1:p.Gly84=
NM_000518.5:c.251_252delinsGC MANE Select NP_000509.1:p.Gly84=