Canonical Allele Identifier: CA2200882941
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176887C= , CM000678.2:g.176887C= GRCh38
NC_000016.9:g.226886C= , CM000678.1:g.226886C= GRCh37
NC_000016.8:g.166886C= NCBI36
NG_000006.1:g.37750C=
NG_059186.1:g.5237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.96-42C= MANE Select ENSP00000322421.5:n.96-42C=
ENST00000397797.1:c.-1-42C= ENSP00000380899.1:n.-1-42C=
ENST00000472694.1:n.190C=
ENST00000487791.1:n.65-42C=
NM_000558.4:c.96-42C= NP_000549.1:n.96-42C=
NM_000558.5:c.96-42C= MANE Select NP_000549.1:n.96-42C=