Canonical Allele Identifier: CA276414328
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs281860608
MyVariant Identifiers: chr16:g.222940A>C (hg19) chr16:g.172941A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172941A>C , CM000678.2:g.172941A>C GRCh38
NC_000016.9:g.222940A>C , CM000678.1:g.222940A>C GRCh37
NC_000016.8:g.162940A>C NCBI36
NG_000006.1:g.33804A>C
NG_059186.1:g.1291A>C
NG_059271.1:g.5095A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.29A>C MANE Select ENSP00000251595.6:p.Asn10Thr
ENST00000251595.10:c.29A>C ENSP00000251595.6:p.Asn10Thr
ENST00000397806.1:c.-19A>C ENSP00000380908.1:n.-19A>C
ENST00000482565.1:n.48A>C
NM_000517.4:c.29A>C NP_000508.1:p.Asn10Thr
NM_000517.6:c.29A>C MANE Select NP_000508.1:p.Asn10Thr
Search 100 bp 5'
Search 100 bp 3'