Canonical Allele Identifier: CA276414382
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281864812
MyVariant Identifiers: chr16:g.222961A>C (hg19) chr16:g.172962A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172962A>C , CM000678.2:g.172962A>C GRCh38
NC_000016.9:g.222961A>C , CM000678.1:g.222961A>C GRCh37
NC_000016.8:g.162961A>C NCBI36
NG_000006.1:g.33825A>C
NG_059186.1:g.1312A>C
NG_059271.1:g.5116A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.50A>C MANE Select ENSP00000251595.6:p.Lys17Thr
ENST00000251595.10:c.50A>C ENSP00000251595.6:p.Lys17Thr
ENST00000397806.1:c.-2+4A>C ENSP00000380908.1:n.-2+4A>C
ENST00000482565.1:n.69A>C
ENST00000484216.1:n.19A>C
NM_000517.4:c.50A>C NP_000508.1:p.Lys17Thr
NM_000517.6:c.50A>C MANE Select NP_000508.1:p.Lys17Thr
Search 100 bp 5'
Search 100 bp 3'