Canonical Allele Identifier: CA276414557
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs41497846
MyVariant Identifiers: chr16:g.223135C>A (hg19) chr16:g.173136C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173136C>A , CM000678.2:g.173136C>A GRCh38
NC_000016.9:g.223135C>A , CM000678.1:g.223135C>A GRCh37
NC_000016.8:g.163135C>A NCBI36
NG_000006.1:g.33999C>A
NG_059186.1:g.1486C>A
NG_059271.1:g.5290C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.107C>A MANE Select ENSP00000251595.6:p.Ser36Tyr
ENST00000251595.10:c.107C>A ENSP00000251595.6:p.Ser36Tyr
ENST00000397806.1:c.11C>A ENSP00000380908.1:p.Ser4Tyr
ENST00000482565.1:n.243C>A
ENST00000484216.1:n.76C>A
NM_000517.4:c.107C>A NP_000508.1:p.Ser36Tyr
NM_000517.6:c.107C>A MANE Select NP_000508.1:p.Ser36Tyr
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