Canonical Allele Identifier: CA2579829612

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249891T= , CM000673.2:g.5249891T= GRCh38
NC_000011.9:g.5271121T= , CM000673.1:g.5271121T= GRCh37
NC_000011.8:g.5227697T= NCBI36
NG_000007.3:g.47725A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1404A= ENSP00000495346.1:n.316-1404A=
ENST00000647543.1:c.379-1404A= ENSP00000496470.1:n.379-1404A=
ENST00000330597.3:c.-87A= (HBG1) ENSP00000327431.3:n.-87A=
ENST00000620888.4:c.316-1404A= (HBG2) ENSP00000479637.1:n.316-1404A=