Canonical Allele Identifier: CA276416757
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs33966883

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176986C>G , CM000678.2:g.176986C>G GRCh38
NC_000016.9:g.226985C>G , CM000678.1:g.226985C>G GRCh37
NC_000016.8:g.166985C>G NCBI36
NG_000006.1:g.37849C>G
NG_059186.1:g.5336C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.153C>G MANE Select ENSP00000322421.5:p.His51Gln
ENST00000397797.1:c.57C>G ENSP00000380899.1:p.His19Gln
ENST00000472694.1:n.289C>G
ENST00000487791.1:n.122C>G
NM_000558.4:c.153C>G NP_000549.1:p.His51Gln
NM_000558.5:c.153C>G MANE Select NP_000549.1:p.His51Gln