Canonical Allele Identifier: CA2200880684
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173202G= , CM000678.2:g.173202G= GRCh38
NC_000016.9:g.223201G= , CM000678.1:g.223201G= GRCh37
NC_000016.8:g.163201G= NCBI36
NG_000006.1:g.34065G=
NG_059186.1:g.1552G=
NG_059271.1:g.5356G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.173G= MANE Select ENSP00000251595.6:p.Gly58=
ENST00000251595.10:c.173G= ENSP00000251595.6:p.Gly58=
ENST00000397806.1:c.77G= ENSP00000380908.1:p.Gly26=
ENST00000482565.1:n.309G=
ENST00000484216.1:n.142G=
NM_000517.4:c.173G= NP_000508.1:p.Gly58=
NM_000517.6:c.173G= MANE Select NP_000508.1:p.Gly58=