Canonical Allele Identifier: CA1949567266
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226574_5226575delinsCA , CM000673.2:g.5226574_5226575delinsCA GRCh38
NC_000011.9:g.5247804_5247805delinsCA , CM000673.1:g.5247804_5247805delinsCA GRCh37
NC_000011.8:g.5204380_5204381delinsCA NCBI36
NG_000007.3:g.71041_71042delinsTG
NG_059281.1:g.5497_5498delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+2_315+3delinsTG ENSP00000494175.1:n.315+2_315+3delinsTG
ENST00000335295.4:c.315+2_315+3delinsTG MANE Select ENSP00000333994.3:n.315+2_315+3delinsTG
ENST00000475226.1:n.247+2_247+3delinsTG
ENST00000485743.1:n.368_369delinsTG
ENST00000633227.1:c.*131+2_*131+3delinsTG ENSP00000488004.1:n.*131+2_*131+3delinsTG...
NM_000518.4:c.315+2_315+3delinsTG NP_000509.1:n.315+2_315+3delinsTG
NM_000518.5:c.315+2_315+3delinsTG MANE Select NP_000509.1:n.315+2_315+3delinsTG