Canonical Allele Identifier: CA492994534
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.227012C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177013C>G , CM000678.2:g.177013C>G GRCh38
NC_000016.9:g.227012C>G , CM000678.1:g.227012C>G GRCh37
NC_000016.8:g.167012C>G NCBI36
NG_000006.1:g.37876C>G
NG_059186.1:g.5363C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.180C>G MANE Select ENSP00000322421.5:p.Gly60=
ENST00000397797.1:c.84C>G ENSP00000380899.1:p.Gly28=
ENST00000472694.1:n.316C>G
ENST00000487791.1:n.149C>G
NM_000558.4:c.180C>G NP_000549.1:p.Gly60=
NM_000558.5:c.180C>G MANE Select NP_000549.1:p.Gly60=
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