Canonical Allele Identifier: CA2200880668
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173180C= , CM000678.2:g.173180C= GRCh38
NC_000016.9:g.223179C= , CM000678.1:g.223179C= GRCh37
NC_000016.8:g.163179C= NCBI36
NG_000006.1:g.34043C=
NG_059186.1:g.1530C=
NG_059271.1:g.5334C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.151C= MANE Select ENSP00000251595.6:p.His51=
ENST00000251595.10:c.151C= ENSP00000251595.6:p.His51=
ENST00000397806.1:c.55C= ENSP00000380908.1:p.His19=
ENST00000482565.1:n.287C=
ENST00000484216.1:n.120C=
NM_000517.4:c.151C= NP_000508.1:p.His51=
NM_000517.6:c.151C= MANE Select NP_000508.1:p.His51=