Canonical Allele Identifier: CA2200882880
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176809G= , CM000678.2:g.176809G= GRCh38
NC_000016.9:g.226808G= , CM000678.1:g.226808G= GRCh37
NC_000016.8:g.166808G= NCBI36
NG_000006.1:g.37672G=
NG_059186.1:g.5159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.93G= MANE Select ENSP00000322421.5:p.Glu31=
ENST00000397797.1:c.-2+47G= ENSP00000380899.1:n.-2+47G=
ENST00000472694.1:n.112G=
ENST00000487791.1:n.62G=
NM_000558.4:c.93G= NP_000549.1:p.Glu31=
NM_000558.5:c.93G= MANE Select NP_000549.1:p.Glu31=