Canonical Allele Identifier: CA492994591
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173185-C-A
MyVariant Identifiers: chr16:g.223184C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173185C>A , CM000678.2:g.173185C>A GRCh38
NC_000016.9:g.223184C>A , CM000678.1:g.223184C>A GRCh37
NC_000016.8:g.163184C>A NCBI36
NG_000006.1:g.34048C>A
NG_059186.1:g.1535C>A
NG_059271.1:g.5339C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.156C>A MANE Select ENSP00000251595.6:p.Gly52=
ENST00000251595.10:c.156C>A ENSP00000251595.6:p.Gly52=
ENST00000397806.1:c.60C>A ENSP00000380908.1:p.Gly20=
ENST00000482565.1:n.292C>A
ENST00000484216.1:n.125C>A
NM_000517.4:c.156C>A NP_000508.1:p.Gly52=
NM_000517.6:c.156C>A MANE Select NP_000508.1:p.Gly52=