Canonical Allele Identifier: CA2630739367
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176869-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176869A>G , CM000678.2:g.176869A>G GRCh38
NC_000016.9:g.226868A>G , CM000678.1:g.226868A>G GRCh37
NC_000016.8:g.166868A>G NCBI36
NG_000006.1:g.37732A>G
NG_059186.1:g.5219A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.95+58A>G MANE Select ENSP00000322421.5:n.95+58A>G
ENST00000397797.1:c.-1-60A>G ENSP00000380899.1:n.-1-60A>G
ENST00000472694.1:n.172A>G
ENST00000487791.1:n.64+58A>G
NM_000558.4:c.95+58A>G NP_000549.1:n.95+58A>G
NM_000558.5:c.95+58A>G MANE Select NP_000549.1:n.95+58A>G