Canonical Allele Identifier: CA492994737
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.227126C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177127C>T , CM000678.2:g.177127C>T GRCh38
NC_000016.9:g.227126C>T , CM000678.1:g.227126C>T GRCh37
NC_000016.8:g.167126C>T NCBI36
NG_000006.1:g.37990C>T
NG_059186.1:g.5477C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.294C>T MANE Select ENSP00000322421.5:p.Asn98=
ENST00000397797.1:c.198C>T ENSP00000380899.1:p.Asn66=
ENST00000472694.1:n.430C>T
ENST00000487791.1:n.263C>T
NM_000558.4:c.294C>T NP_000549.1:p.Asn98=
NM_000558.5:c.294C>T MANE Select NP_000549.1:p.Asn98=