Canonical Allele Identifier: CA125711
Gene: HBA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 15719
ClinVar RCV Id: RCV000017013
dbSNP Id: rs35859529

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177051A>G , CM000678.2:g.177051A>G GRCh38
NC_000016.9:g.227050A>G , CM000678.1:g.227050A>G GRCh37
NC_000016.8:g.167050A>G NCBI36
NG_000006.1:g.37914A>G
NG_059186.1:g.5401A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.218A>G MANE Select ENSP00000322421.5:p.His73Arg
ENST00000397797.1:c.122A>G ENSP00000380899.1:p.His41Arg
ENST00000472694.1:n.354A>G
ENST00000487791.1:n.187A>G
NM_000558.4:c.218A>G NP_000549.1:p.His73Arg
NM_000558.5:c.218A>G MANE Select NP_000549.1:p.His73Arg