Canonical Allele Identifier: CA492785190
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223500G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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