Canonical Allele Identifier: CA393994996
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs750867079
gnomAD v2: 16-226790-T-G
gnomAD v3: 16-176791-T-G
gnomAD v4: 16-176791-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176791T>G , CM000678.2:g.176791T>G GRCh38
NC_000016.9:g.226790T>G , CM000678.1:g.226790T>G GRCh37
NC_000016.8:g.166790T>G NCBI36
NG_000006.1:g.37654T>G
NG_059186.1:g.5141T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.75T>G MANE Select ENSP00000322421.5:p.Tyr25Ter
ENST00000397797.1:c.-2+29T>G ENSP00000380899.1:n.-2+29T>G
ENST00000472694.1:n.94T>G
ENST00000487791.1:n.44T>G
NM_000558.4:c.75T>G NP_000549.1:p.Tyr25Ter
NM_000558.5:c.75T>G MANE Select NP_000549.1:p.Tyr25Ter