Canonical Allele Identifier: CA393993482
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173211A>G , CM000678.2:g.173211A>G GRCh38
NC_000016.9:g.223210A>G , CM000678.1:g.223210A>G GRCh37
NC_000016.8:g.163210A>G NCBI36
NG_000006.1:g.34074A>G
NG_059186.1:g.1561A>G
NG_059271.1:g.5365A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.182A>G MANE Select ENSP00000251595.6:p.Lys61Arg
ENST00000251595.10:c.182A>G ENSP00000251595.6:p.Lys61Arg
ENST00000397806.1:c.86A>G ENSP00000380908.1:p.Lys29Arg
ENST00000482565.1:n.318A>G
ENST00000484216.1:n.151A>G
NM_000517.4:c.182A>G NP_000508.1:p.Lys61Arg
NM_000517.6:c.182A>G MANE Select NP_000508.1:p.Lys61Arg