Canonical Allele Identifier: CA393994989
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176787A>C , CM000678.2:g.176787A>C GRCh38
NC_000016.9:g.226786A>C , CM000678.1:g.226786A>C GRCh37
NC_000016.8:g.166786A>C NCBI36
NG_000006.1:g.37650A>C
NG_059186.1:g.5137A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.71A>C MANE Select ENSP00000322421.5:p.Glu24Ala
ENST00000397797.1:c.-2+25A>C ENSP00000380899.1:n.-2+25A>C
ENST00000472694.1:n.90A>C
ENST00000487791.1:n.40A>C
NM_000558.4:c.71A>C NP_000549.1:p.Glu24Ala
NM_000558.5:c.71A>C MANE Select NP_000549.1:p.Glu24Ala