Canonical Allele Identifier: CA276414778
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864849
MyVariant Identifiers: chr16:g.223221G>T (hg19) chr16:g.173222G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173222G>T , CM000678.2:g.173222G>T GRCh38
NC_000016.9:g.223221G>T , CM000678.1:g.223221G>T GRCh37
NC_000016.8:g.163221G>T NCBI36
NG_000006.1:g.34085G>T
NG_059186.1:g.1572G>T
NG_059271.1:g.5376G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.193G>T MANE Select ENSP00000251595.6:p.Asp65Tyr
ENST00000251595.10:c.193G>T ENSP00000251595.6:p.Asp65Tyr
ENST00000397806.1:c.97G>T ENSP00000380908.1:p.Asp33Tyr
ENST00000482565.1:n.329G>T
ENST00000484216.1:n.162G>T
NM_000517.4:c.193G>T NP_000508.1:p.Asp65Tyr
NM_000517.6:c.193G>T MANE Select NP_000508.1:p.Asp65Tyr
Search 100 bp 5'
Search 100 bp 3'