Canonical Allele Identifier: CA2200880593
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173083C= , CM000678.2:g.173083C= GRCh38
NC_000016.9:g.223082C= , CM000678.1:g.223082C= GRCh37
NC_000016.8:g.163082C= NCBI36
NG_000006.1:g.33946C=
NG_059186.1:g.1433C=
NG_059271.1:g.5237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-42C= MANE Select ENSP00000251595.6:n.96-42C=
ENST00000251595.10:c.96-42C= ENSP00000251595.6:n.96-42C=
ENST00000397806.1:c.-1-42C= ENSP00000380908.1:n.-1-42C=
ENST00000482565.1:n.190C=
ENST00000484216.1:n.65-42C=
NM_000517.4:c.96-42C= NP_000508.1:n.96-42C=
NM_000517.6:c.96-42C= MANE Select NP_000508.1:n.96-42C=