Canonical Allele Identifier: CA492785195
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1276938524
gnomAD v3: 16-173501-G-A
gnomAD v4: 16-173501-G-A
MyVariant Identifiers: chr16:g.223500G>A (hg19) chr16:g.173501G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173501G>A , CM000678.2:g.173501G>A GRCh38
NC_000016.9:g.223500G>A , CM000678.1:g.223500G>A GRCh37
NC_000016.8:g.163500G>A NCBI36
NG_000006.1:g.34364G>A
NG_059186.1:g.1851G>A
NG_059271.1:g.5655G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.330G>A MANE Select ENSP00000251595.6:p.Leu110=
ENST00000251595.10:c.330G>A ENSP00000251595.6:p.Leu110=
ENST00000397806.1:c.234G>A ENSP00000380908.1:p.Leu78=
ENST00000482565.1:n.466G>A
NM_000517.4:c.330G>A NP_000508.1:p.Leu110=
NM_000517.6:c.330G>A MANE Select NP_000508.1:p.Leu110=
Search 100 bp 5'
Search 100 bp 3'