Canonical Allele Identifier: CA393994987
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176784G>C , CM000678.2:g.176784G>C GRCh38
NC_000016.9:g.226783G>C , CM000678.1:g.226783G>C GRCh37
NC_000016.8:g.166783G>C NCBI36
NG_000006.1:g.37647G>C
NG_059186.1:g.5134G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.68G>C MANE Select ENSP00000322421.5:p.Gly23Ala
ENST00000397797.1:c.-2+22G>C ENSP00000380899.1:n.-2+22G>C
ENST00000472694.1:n.87G>C
ENST00000487791.1:n.37G>C
NM_000558.4:c.68G>C NP_000549.1:p.Gly23Ala
NM_000558.5:c.68G>C MANE Select NP_000549.1:p.Gly23Ala