Canonical Allele Identifier: CA1949583557

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249402C= , CM000673.2:g.5249402C= GRCh38
NC_000011.9:g.5270632C= , CM000673.1:g.5270632C= GRCh37
NC_000011.8:g.5227208C= NCBI36
NG_000007.3:g.48214G=

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.281G= (HBG1) MANE Select ENSP00000327431.4:p.Cys94=
ENST00000642908.1:c.316-915G= ENSP00000495346.1:n.316-915G=
ENST00000647543.1:c.379-915G= ENSP00000496470.1:n.379-915G=
ENST00000648735.1:n.332G= (HBG1)
ENST00000330597.3:c.281G= (HBG1) ENSP00000327431.3:p.Cys94=
ENST00000620888.4:c.316-915G= (HBG2) ENSP00000479637.1:n.316-915G=
ENST00000623781.1:c.74C= ENSP00000485381.1:p.Thr25=
ENST00000632727.1:c.*150G= (HBG1) ENSP00000488759.1:n.*150G=
NM_000559.2:c.281G= (HBG1) NP_000550.2:p.Cys94=
NM_000559.3:c.281G= (HBG1) MANE Select NP_000550.2:p.Cys94=