Canonical Allele Identifier: CA2200880823
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173387G= , CM000678.2:g.173387G= GRCh38
NC_000016.9:g.223386G= , CM000678.1:g.223386G= GRCh37
NC_000016.8:g.163386G= NCBI36
NG_000006.1:g.34250G=
NG_059186.1:g.1737G=
NG_059271.1:g.5541G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.300+58G= MANE Select ENSP00000251595.6:n.300+58G=
ENST00000251595.10:c.300+58G= ENSP00000251595.6:n.300+58G=
ENST00000397806.1:c.204+58G= ENSP00000380908.1:n.204+58G=
ENST00000482565.1:n.436+58G=
ENST00000484216.1:n.327G=
NM_000517.4:c.300+58G= NP_000508.1:n.300+58G=
NM_000517.6:c.300+58G= MANE Select NP_000508.1:n.300+58G=