Canonical Allele Identifier: CA492994241
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.222992G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172993G>A , CM000678.2:g.172993G>A GRCh38
NC_000016.9:g.222992G>A , CM000678.1:g.222992G>A GRCh37
NC_000016.8:g.162992G>A NCBI36
NG_000006.1:g.33856G>A
NG_059186.1:g.1343G>A
NG_059271.1:g.5147G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.81G>A MANE Select ENSP00000251595.6:p.Ala27=
ENST00000251595.10:c.81G>A ENSP00000251595.6:p.Ala27=
ENST00000397806.1:c.-2+35G>A ENSP00000380908.1:n.-2+35G>A
ENST00000482565.1:n.100G>A
ENST00000484216.1:n.50G>A
NM_000517.4:c.81G>A NP_000508.1:p.Ala27=
NM_000517.6:c.81G>A MANE Select NP_000508.1:p.Ala27=
Search 100 bp 5'
Search 100 bp 3'