Canonical Allele Identifier: CA2200880748
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173286A= , CM000678.2:g.173286A= GRCh38
NC_000016.9:g.223285A= , CM000678.1:g.223285A= GRCh37
NC_000016.8:g.163285A= NCBI36
NG_000006.1:g.34149A=
NG_059186.1:g.1636A=
NG_059271.1:g.5440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.257A= MANE Select ENSP00000251595.6:p.Asp86=
ENST00000251595.10:c.257A= ENSP00000251595.6:p.Asp86=
ENST00000397806.1:c.161A= ENSP00000380908.1:p.Asp54=
ENST00000482565.1:n.393A=
ENST00000484216.1:n.226A=
NM_000517.4:c.257A= NP_000508.1:p.Asp86=
NM_000517.6:c.257A= MANE Select NP_000508.1:p.Asp86=