Canonical Allele Identifier: CA2200880854
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173430C= , CM000678.2:g.173430C= GRCh38
NC_000016.9:g.223429C= , CM000678.1:g.223429C= GRCh37
NC_000016.8:g.163429C= NCBI36
NG_000006.1:g.34293C=
NG_059186.1:g.1780C=
NG_059271.1:g.5584C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.301-42C= MANE Select ENSP00000251595.6:n.301-42C=
ENST00000251595.10:c.301-42C= ENSP00000251595.6:n.301-42C=
ENST00000397806.1:c.205-42C= ENSP00000380908.1:n.205-42C=
ENST00000482565.1:n.437-42C=
ENST00000484216.1:n.370C=
NM_000517.4:c.301-42C= NP_000508.1:n.301-42C=
NM_000517.6:c.301-42C= MANE Select NP_000508.1:n.301-42C=