Canonical Allele Identifier: CA1949564731
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225662_5225664delinsACT , CM000673.2:g.5225662_5225664delinsACT GRCh38
NC_000011.9:g.5246892_5246894delinsACT , CM000673.1:g.5246892_5246894delinsACT GRCh37
NC_000011.8:g.5203468_5203470delinsACT NCBI36
NG_000007.3:g.71952_71954delinsAGT
NG_059281.1:g.6408_6410delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.378_380delinsAGT ENSP00000494175.1:p.Pro126=
ENST00000335295.4:c.378_380delinsAGT MANE Select ENSP00000333994.3:p.Pro126=
ENST00000475226.1:n.310_312delinsAGT
ENST00000633227.1:c.*194_*196delinsAGT ENSP00000488004.1:n.*194_*196delinsAGT
NM_000518.4:c.378_380delinsAGT NP_000509.1:p.Pro126=
NM_000518.5:c.378_380delinsAGT MANE Select NP_000509.1:p.Pro126=