Canonical Allele Identifier: CA276414851
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864857

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173252G>A , CM000678.2:g.173252G>A GRCh38
NC_000016.9:g.223251G>A , CM000678.1:g.223251G>A GRCh37
NC_000016.8:g.163251G>A NCBI36
NG_000006.1:g.34115G>A
NG_059186.1:g.1602G>A
NG_059271.1:g.5406G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.223G>A MANE Select ENSP00000251595.6:p.Asp75Asn
ENST00000251595.10:c.223G>A ENSP00000251595.6:p.Asp75Asn
ENST00000397806.1:c.127G>A ENSP00000380908.1:p.Asp43Asn
ENST00000482565.1:n.359G>A
ENST00000484216.1:n.192G>A
NM_000517.4:c.223G>A NP_000508.1:p.Asp75Asn
NM_000517.6:c.223G>A MANE Select NP_000508.1:p.Asp75Asn