Canonical Allele Identifier: CA2200880681
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173199A= , CM000678.2:g.173199A= GRCh38
NC_000016.9:g.223198A= , CM000678.1:g.223198A= GRCh37
NC_000016.8:g.163198A= NCBI36
NG_000006.1:g.34062A=
NG_059186.1:g.1549A=
NG_059271.1:g.5353A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.170A= MANE Select ENSP00000251595.6:p.Lys57=
ENST00000251595.10:c.170A= ENSP00000251595.6:p.Lys57=
ENST00000397806.1:c.74A= ENSP00000380908.1:p.Lys25=
ENST00000482565.1:n.306A=
ENST00000484216.1:n.139A=
NM_000517.4:c.170A= NP_000508.1:p.Lys57=
NM_000517.6:c.170A= MANE Select NP_000508.1:p.Lys57=