Canonical Allele Identifier: CA393994642
Gene: HBA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.223573A>C (hg19) chr16:g.173574A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173574A>C , CM000678.2:g.173574A>C GRCh38
NC_000016.9:g.223573A>C , CM000678.1:g.223573A>C GRCh37
NC_000016.8:g.163573A>C NCBI36
NG_000006.1:g.34437A>C
NG_059186.1:g.1924A>C
NG_059271.1:g.5728A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.403A>C MANE Select ENSP00000251595.6:p.Thr135Pro
ENST00000251595.10:c.403A>C ENSP00000251595.6:p.Thr135Pro
ENST00000397806.1:c.307A>C ENSP00000380908.1:p.Thr103Pro
ENST00000482565.1:n.539A>C
NM_000517.4:c.403A>C NP_000508.1:p.Thr135Pro
NM_000517.6:c.403A>C MANE Select NP_000508.1:p.Thr135Pro
Search 100 bp 5'
Search 100 bp 3'