Canonical Allele Identifier: CA718606267
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1159661188
gnomAD v3: 16-176876-A-G
gnomAD v4: 16-176876-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176876A>G , CM000678.2:g.176876A>G GRCh38
NC_000016.9:g.226875A>G , CM000678.1:g.226875A>G GRCh37
NC_000016.8:g.166875A>G NCBI36
NG_000006.1:g.37739A>G
NG_059186.1:g.5226A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-53A>G MANE Select ENSP00000322421.5:n.96-53A>G
ENST00000397797.1:c.-1-53A>G ENSP00000380899.1:n.-1-53A>G
ENST00000472694.1:n.179A>G
ENST00000487791.1:n.65-53A>G
NM_000558.4:c.96-53A>G NP_000549.1:n.96-53A>G
NM_000558.5:c.96-53A>G MANE Select NP_000549.1:n.96-53A>G