Canonical Allele Identifier: CA492785601
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223584C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173585C>G , CM000678.2:g.173585C>G GRCh38
NC_000016.9:g.223584C>G , CM000678.1:g.223584C>G GRCh37
NC_000016.8:g.163584C>G NCBI36
NG_000006.1:g.34448C>G
NG_059186.1:g.1935C>G
NG_059271.1:g.5739C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.414C>G MANE Select ENSP00000251595.6:p.Thr138=
ENST00000251595.10:c.414C>G ENSP00000251595.6:p.Thr138=
ENST00000397806.1:c.318C>G ENSP00000380908.1:p.Thr106=
ENST00000482565.1:n.550C>G
NM_000517.4:c.414C>G NP_000508.1:p.Thr138=
NM_000517.6:c.414C>G MANE Select NP_000508.1:p.Thr138=
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