Canonical Allele Identifier: CA492994551
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-177025-C-T
MyVariant Identifiers: chr16:g.227024C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177025C>T , CM000678.2:g.177025C>T GRCh38
NC_000016.9:g.227024C>T , CM000678.1:g.227024C>T GRCh37
NC_000016.8:g.167024C>T NCBI36
NG_000006.1:g.37888C>T
NG_059186.1:g.5375C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.192C>T MANE Select ENSP00000322421.5:p.Ala64=
ENST00000397797.1:c.96C>T ENSP00000380899.1:p.Ala32=
ENST00000472694.1:n.328C>T
ENST00000487791.1:n.161C>T
NM_000558.4:c.192C>T NP_000549.1:p.Ala64=
NM_000558.5:c.192C>T MANE Select NP_000549.1:p.Ala64=
Search 100 bp 5'
Search 100 bp 3'