Canonical Allele Identifier: CA393995774
Gene: HBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177292C>G , CM000678.2:g.177292C>G GRCh38
NC_000016.9:g.227291C>G , CM000678.1:g.227291C>G GRCh37
NC_000016.8:g.167291C>G NCBI36
NG_000006.1:g.38155C>G
NG_059186.1:g.5642C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.310C>G MANE Select ENSP00000322421.5:p.His104Asp
ENST00000397797.1:c.214C>G ENSP00000380899.1:p.His72Asp
ENST00000472694.1:n.446C>G
NM_000558.4:c.310C>G NP_000549.1:p.His104Asp
NM_000558.5:c.310C>G MANE Select NP_000549.1:p.His104Asp