Canonical Allele Identifier: CA276414401
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs63750679
MyVariant Identifiers: chr16:g.222967G>A (hg19) chr16:g.172968G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172968G>A , CM000678.2:g.172968G>A GRCh38
NC_000016.9:g.222967G>A , CM000678.1:g.222967G>A GRCh37
NC_000016.8:g.162967G>A NCBI36
NG_000006.1:g.33831G>A
NG_059186.1:g.1318G>A
NG_059271.1:g.5122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.56G>A MANE Select ENSP00000251595.6:p.Gly19Asp
ENST00000251595.10:c.56G>A ENSP00000251595.6:p.Gly19Asp
ENST00000397806.1:c.-2+10G>A ENSP00000380908.1:n.-2+10G>A
ENST00000482565.1:n.75G>A
ENST00000484216.1:n.25G>A
NM_000517.4:c.56G>A NP_000508.1:p.Gly19Asp
NM_000517.6:c.56G>A MANE Select NP_000508.1:p.Gly19Asp
Search 100 bp 5'
Search 100 bp 3'