Canonical Allele Identifier: CA393995787
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177296G>C , CM000678.2:g.177296G>C GRCh38
NC_000016.9:g.227295G>C , CM000678.1:g.227295G>C GRCh37
NC_000016.8:g.167295G>C NCBI36
NG_000006.1:g.38159G>C
NG_059186.1:g.5646G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.314G>C MANE Select ENSP00000322421.5:p.Cys105Ser
ENST00000397797.1:c.218G>C ENSP00000380899.1:p.Cys73Ser
ENST00000472694.1:n.450G>C
NM_000558.4:c.314G>C NP_000549.1:p.Cys105Ser
NM_000558.5:c.314G>C MANE Select NP_000549.1:p.Cys105Ser