Canonical Allele Identifier: CA2630738749
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176702-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176702C>T , CM000678.2:g.176702C>T GRCh38
NC_000016.9:g.226701C>T , CM000678.1:g.226701C>T GRCh37
NC_000016.8:g.166701C>T NCBI36
NG_000006.1:g.37565C>T
NG_059186.1:g.5052C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-15C>T MANE Select ENSP00000322421.5:n.-15C>T
ENST00000472694.1:n.5C>T
NM_000558.4:c.-15C>T NP_000549.1:n.-15C>T
NM_000558.5:c.-15C>T MANE Select NP_000549.1:n.-15C>T