Canonical Allele Identifier: CA125567
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 15635
dbSNP Id: rs281865555
gnomAD v4: 16-172961-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172961A>G , CM000678.2:g.172961A>G GRCh38
NC_000016.9:g.222960A>G , CM000678.1:g.222960A>G GRCh37
NC_000016.8:g.162960A>G NCBI36
NG_000006.1:g.33824A>G
NG_059186.1:g.1311A>G
NG_059271.1:g.5115A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.49A>G MANE Select ENSP00000251595.6:p.Lys17Glu
ENST00000251595.10:c.49A>G ENSP00000251595.6:p.Lys17Glu
ENST00000397806.1:c.-2+3A>G ENSP00000380908.1:n.-2+3A>G
ENST00000482565.1:n.68A>G
ENST00000484216.1:n.18A>G
NM_000517.4:c.49A>G NP_000508.1:p.Lys17Glu
NM_000517.6:c.49A>G MANE Select NP_000508.1:p.Lys17Glu