Canonical Allele Identifier: CA2630738628
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176660-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176660T>C , CM000678.2:g.176660T>C GRCh38
NC_000016.9:g.226659T>C , CM000678.1:g.226659T>C GRCh37
NC_000016.8:g.166659T>C NCBI36
NG_000006.1:g.37523T>C
NG_059186.1:g.5010T>C

Transcript Alleles

HGVS Amino-acid change
NM_000558.4:c.-57T>C NP_000549.1:n.-57T>C