Canonical Allele Identifier: CA2200882782
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176692C= , CM000678.2:g.176692C= GRCh38
NC_000016.9:g.226691C= , CM000678.1:g.226691C= GRCh37
NC_000016.8:g.166691C= NCBI36
NG_000006.1:g.37555C=
NG_059186.1:g.5042C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-25C= MANE Select ENSP00000322421.5:n.-25C=
NM_000558.4:c.-25C= NP_000549.1:n.-25C=
NM_000558.5:c.-25C= MANE Select NP_000549.1:n.-25C=