Canonical Allele Identifier: CA2200882774
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176684T= , CM000678.2:g.176684T= GRCh38
NC_000016.9:g.226683T= , CM000678.1:g.226683T= GRCh37
NC_000016.8:g.166683T= NCBI36
NG_000006.1:g.37547T=
NG_059186.1:g.5034T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-33T= MANE Select ENSP00000322421.5:n.-33T=
NM_000558.4:c.-33T= NP_000549.1:n.-33T=
NM_000558.5:c.-33T= MANE Select NP_000549.1:n.-33T=