Canonical Allele Identifier: CA1949583539

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249390T= , CM000673.2:g.5249390T= GRCh38
NC_000011.9:g.5270620T= , CM000673.1:g.5270620T= GRCh37
NC_000011.8:g.5227196T= NCBI36
NG_000007.3:g.48226A=

Transcript Alleles

HGVS Amino-acid change
ENST00000330597.5:c.293A= (HBG1) MANE Select ENSP00000327431.4:p.His98=
ENST00000642908.1:c.316-903A= ENSP00000495346.1:n.316-903A=
ENST00000647543.1:c.379-903A= ENSP00000496470.1:n.379-903A=
ENST00000648735.1:n.344A= (HBG1)
ENST00000330597.3:c.293A= (HBG1) ENSP00000327431.3:p.His98=
ENST00000620888.4:c.316-903A= (HBG2) ENSP00000479637.1:n.316-903A=
ENST00000623781.1:c.62T= ENSP00000485381.1:p.Met21=
ENST00000632727.1:c.*162A= (HBG1) ENSP00000488759.1:n.*162A=
NM_000559.2:c.293A= (HBG1) NP_000550.2:p.His98=
NM_000559.3:c.293A= (HBG1) MANE Select NP_000550.2:p.His98=