Canonical Allele Identifier: CA2630736563
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-177514-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177514T>A , CM000678.2:g.177514T>A GRCh38
NC_000016.9:g.227513T>A , CM000678.1:g.227513T>A GRCh37
NC_000016.8:g.167513T>A NCBI36
NG_000006.1:g.38377T>A
NG_059186.1:g.5864T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.*103T>A MANE Select ENSP00000322421.5:n.*103T>A
ENST00000397797.1:c.*103T>A ENSP00000380899.1:n.*103T>A
ENST00000472694.1:n.668T>A
NM_000558.4:c.*103T>A NP_000549.1:n.*103T>A
NM_000558.5:c.*103T>A MANE Select NP_000549.1:n.*103T>A