Canonical Allele Identifier: CA2200882874
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176805T= , CM000678.2:g.176805T= GRCh38
NC_000016.9:g.226804T= , CM000678.1:g.226804T= GRCh37
NC_000016.8:g.166804T= NCBI36
NG_000006.1:g.37668T=
NG_059186.1:g.5155T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.89T= MANE Select ENSP00000322421.5:p.Leu30=
ENST00000397797.1:c.-2+43T= ENSP00000380899.1:n.-2+43T=
ENST00000472694.1:n.108T=
ENST00000487791.1:n.58T=
NM_000558.4:c.89T= NP_000549.1:p.Leu30=
NM_000558.5:c.89T= MANE Select NP_000549.1:p.Leu30=