Canonical Allele Identifier: CA492994727
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-177121-G-T
MyVariant Identifiers: chr16:g.227120G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177121G>T , CM000678.2:g.177121G>T GRCh38
NC_000016.9:g.227120G>T , CM000678.1:g.227120G>T GRCh37
NC_000016.8:g.167120G>T NCBI36
NG_000006.1:g.37984G>T
NG_059186.1:g.5471G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.288G>T MANE Select ENSP00000322421.5:p.Pro96=
ENST00000397797.1:c.192G>T ENSP00000380899.1:p.Pro64=
ENST00000472694.1:n.424G>T
ENST00000487791.1:n.257G>T
NM_000558.4:c.288G>T NP_000549.1:p.Pro96=
NM_000558.5:c.288G>T MANE Select NP_000549.1:p.Pro96=