Canonical Allele Identifier: CA2200881026
Gene: HBA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173647G= , CM000678.2:g.173647G= GRCh38
NC_000016.9:g.223646G= , CM000678.1:g.223646G= GRCh37
NC_000016.8:g.163646G= NCBI36
NG_000006.1:g.34510G=
NG_059186.1:g.1997G=
NG_059271.1:g.5801G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*47G= MANE Select ENSP00000251595.6:n.*47G=
ENST00000251595.10:c.*47G= ENSP00000251595.6:n.*47G=
ENST00000397806.1:c.*47G= ENSP00000380908.1:n.*47G=
ENST00000482565.1:n.612G=
NM_000517.4:c.*47G= NP_000508.1:n.*47G=
NM_000517.6:c.*47G= MANE Select NP_000508.1:n.*47G=
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