Canonical Allele Identifier: CA2200880683
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173201G= , CM000678.2:g.173201G= GRCh38
NC_000016.9:g.223200G= , CM000678.1:g.223200G= GRCh37
NC_000016.8:g.163200G= NCBI36
NG_000006.1:g.34064G=
NG_059186.1:g.1551G=
NG_059271.1:g.5355G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.172G= MANE Select ENSP00000251595.6:p.Gly58=
ENST00000251595.10:c.172G= ENSP00000251595.6:p.Gly58=
ENST00000397806.1:c.76G= ENSP00000380908.1:p.Gly26=
ENST00000482565.1:n.308G=
ENST00000484216.1:n.141G=
NM_000517.4:c.172G= NP_000508.1:p.Gly58=
NM_000517.6:c.172G= MANE Select NP_000508.1:p.Gly58=