Canonical Allele Identifier: CA2579829532

Linked Data

gnomAD v4: 11-5249863-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249863A>T , CM000673.2:g.5249863A>T GRCh38
NC_000011.9:g.5271093A>T , CM000673.1:g.5271093A>T GRCh37
NC_000011.8:g.5227669A>T NCBI36
NG_000007.3:g.47753T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1376T>A ENSP00000495346.1:n.316-1376T>A
ENST00000647543.1:c.379-1376T>A ENSP00000496470.1:n.379-1376T>A
ENST00000330597.3:c.-59T>A (HBG1) ENSP00000327431.3:n.-59T>A
ENST00000620888.4:c.316-1376T>A (HBG2) ENSP00000479637.1:n.316-1376T>A