Canonical Allele Identifier: CA492994512
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.226997G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176998G>A , CM000678.2:g.176998G>A GRCh38
NC_000016.9:g.226997G>A , CM000678.1:g.226997G>A GRCh37
NC_000016.8:g.166997G>A NCBI36
NG_000006.1:g.37861G>A
NG_059186.1:g.5348G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.165G>A MANE Select ENSP00000322421.5:p.Gln55=
ENST00000397797.1:c.69G>A ENSP00000380899.1:p.Gln23=
ENST00000472694.1:n.301G>A
ENST00000487791.1:n.134G>A
NM_000558.4:c.165G>A NP_000549.1:p.Gln55=
NM_000558.5:c.165G>A MANE Select NP_000549.1:p.Gln55=
Search 100 bp 5'
Search 100 bp 3'