Canonical Allele Identifier: CA276416999
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs33911106

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177105A>G , CM000678.2:g.177105A>G GRCh38
NC_000016.9:g.227104A>G , CM000678.1:g.227104A>G GRCh37
NC_000016.8:g.167104A>G NCBI36
NG_000006.1:g.37968A>G
NG_059186.1:g.5455A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.272A>G MANE Select ENSP00000322421.5:p.Lys91Arg
ENST00000397797.1:c.176A>G ENSP00000380899.1:p.Lys59Arg
ENST00000472694.1:n.408A>G
ENST00000487791.1:n.241A>G
NM_000558.4:c.272A>G NP_000549.1:p.Lys91Arg
NM_000558.5:c.272A>G MANE Select NP_000549.1:p.Lys91Arg