Canonical Allele Identifier: CA492994378
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-177297-C-T
MyVariant Identifiers: chr16:g.227296C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177297C>T , CM000678.2:g.177297C>T GRCh38
NC_000016.9:g.227296C>T , CM000678.1:g.227296C>T GRCh37
NC_000016.8:g.167296C>T NCBI36
NG_000006.1:g.38160C>T
NG_059186.1:g.5647C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.315C>T MANE Select ENSP00000322421.5:p.Cys105=
ENST00000397797.1:c.219C>T ENSP00000380899.1:p.Cys73=
ENST00000472694.1:n.451C>T
NM_000558.4:c.315C>T NP_000549.1:p.Cys105=
NM_000558.5:c.315C>T MANE Select NP_000549.1:p.Cys105=