Canonical Allele Identifier: CA393996033
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177401A>G , CM000678.2:g.177401A>G GRCh38
NC_000016.9:g.227400A>G , CM000678.1:g.227400A>G GRCh37
NC_000016.8:g.167400A>G NCBI36
NG_000006.1:g.38264A>G
NG_059186.1:g.5751A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.419A>G MANE Select ENSP00000322421.5:p.Lys140Arg
ENST00000397797.1:c.323A>G ENSP00000380899.1:p.Lys108Arg
ENST00000472694.1:n.555A>G
NM_000558.4:c.419A>G NP_000549.1:p.Lys140Arg
NM_000558.5:c.419A>G MANE Select NP_000549.1:p.Lys140Arg