Canonical Allele Identifier: CA276415508
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864488
MyVariant Identifiers: chr16:g.223574C>G (hg19) chr16:g.173575C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173575C>G , CM000678.2:g.173575C>G GRCh38
NC_000016.9:g.223574C>G , CM000678.1:g.223574C>G GRCh37
NC_000016.8:g.163574C>G NCBI36
NG_000006.1:g.34438C>G
NG_059186.1:g.1925C>G
NG_059271.1:g.5729C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.404C>G MANE Select ENSP00000251595.6:p.Thr135Ser
ENST00000251595.10:c.404C>G ENSP00000251595.6:p.Thr135Ser
ENST00000397806.1:c.308C>G ENSP00000380908.1:p.Thr103Ser
ENST00000482565.1:n.540C>G
NM_000517.4:c.404C>G NP_000508.1:p.Thr135Ser
NM_000517.6:c.404C>G MANE Select NP_000508.1:p.Thr135Ser
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Search 100 bp 3'