Canonical Allele Identifier: CA492994555
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902044086
MyVariant Identifiers: chr16:g.223163G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173164G>A , CM000678.2:g.173164G>A GRCh38
NC_000016.9:g.223163G>A , CM000678.1:g.223163G>A GRCh37
NC_000016.8:g.163163G>A NCBI36
NG_000006.1:g.34027G>A
NG_059186.1:g.1514G>A
NG_059271.1:g.5318G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.135G>A MANE Select ENSP00000251595.6:p.Pro45=
ENST00000251595.10:c.135G>A ENSP00000251595.6:p.Pro45=
ENST00000397806.1:c.39G>A ENSP00000380908.1:p.Pro13=
ENST00000482565.1:n.271G>A
ENST00000484216.1:n.104G>A
NM_000517.4:c.135G>A NP_000508.1:p.Pro45=
NM_000517.6:c.135G>A MANE Select NP_000508.1:p.Pro45=
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