Canonical Allele Identifier: CA1949584166

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249888T= , CM000673.2:g.5249888T= GRCh38
NC_000011.9:g.5271118T= , CM000673.1:g.5271118T= GRCh37
NC_000011.8:g.5227694T= NCBI36
NG_000007.3:g.47728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1401A= ENSP00000495346.1:n.316-1401A=
ENST00000647543.1:c.379-1401A= ENSP00000496470.1:n.379-1401A=
ENST00000330597.3:c.-84A= (HBG1) ENSP00000327431.3:n.-84A=
ENST00000620888.4:c.316-1401A= (HBG2) ENSP00000479637.1:n.316-1401A=