Canonical Allele Identifier: CA393994982
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176780-G-T
MyVariant Identifiers: chr16:g.226779G>T (hg19) chr16:g.176780G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176780G>T , CM000678.2:g.176780G>T GRCh38
NC_000016.9:g.226779G>T , CM000678.1:g.226779G>T GRCh37
NC_000016.8:g.166779G>T NCBI36
NG_000006.1:g.37643G>T
NG_059186.1:g.5130G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.64G>T MANE Select ENSP00000322421.5:p.Ala22Ser
ENST00000397797.1:c.-2+18G>T ENSP00000380899.1:n.-2+18G>T
ENST00000472694.1:n.83G>T
ENST00000487791.1:n.33G>T
NM_000558.4:c.64G>T NP_000549.1:p.Ala22Ser
NM_000558.5:c.64G>T MANE Select NP_000549.1:p.Ala22Ser
Search 100 bp 5'
Search 100 bp 3'