Canonical Allele Identifier: CA2630738717
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176683-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176683C>G , CM000678.2:g.176683C>G GRCh38
NC_000016.9:g.226682C>G , CM000678.1:g.226682C>G GRCh37
NC_000016.8:g.166682C>G NCBI36
NG_000006.1:g.37546C>G
NG_059186.1:g.5033C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.-34C>G MANE Select ENSP00000322421.5:n.-34C>G
NM_000558.4:c.-34C>G NP_000549.1:n.-34C>G
NM_000558.5:c.-34C>G MANE Select NP_000549.1:n.-34C>G