Canonical Allele Identifier: CA492785664
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223596T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173597T>C , CM000678.2:g.173597T>C GRCh38
NC_000016.9:g.223596T>C , CM000678.1:g.223596T>C GRCh37
NC_000016.8:g.163596T>C NCBI36
NG_000006.1:g.34460T>C
NG_059186.1:g.1947T>C
NG_059271.1:g.5751T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.426T>C MANE Select ENSP00000251595.6:p.Arg142=
ENST00000251595.10:c.426T>C ENSP00000251595.6:p.Arg142=
ENST00000397806.1:c.330T>C ENSP00000380908.1:p.Arg110=
ENST00000482565.1:n.562T>C
NM_000517.4:c.426T>C NP_000508.1:p.Arg142=
NM_000517.6:c.426T>C MANE Select NP_000508.1:p.Arg142=
Search 100 bp 5'
Search 100 bp 3'