Canonical Allele Identifier: CA2630738644
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1902140052
gnomAD v4: 16-176663-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176663C>T , CM000678.2:g.176663C>T GRCh38
NC_000016.9:g.226662C>T , CM000678.1:g.226662C>T GRCh37
NC_000016.8:g.166662C>T NCBI36
NG_000006.1:g.37526C>T
NG_059186.1:g.5013C>T

Transcript Alleles

HGVS Amino-acid change
NM_000558.4:c.-54C>T NP_000549.1:n.-54C>T