Canonical Allele Identifier: CA276414727
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs41328049
MyVariant Identifiers: chr16:g.223206G>A (hg19) chr16:g.173207G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173207G>A , CM000678.2:g.173207G>A GRCh38
NC_000016.9:g.223206G>A , CM000678.1:g.223206G>A GRCh37
NC_000016.8:g.163206G>A NCBI36
NG_000006.1:g.34070G>A
NG_059186.1:g.1557G>A
NG_059271.1:g.5361G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.178G>A MANE Select ENSP00000251595.6:p.Gly60Ser
ENST00000251595.10:c.178G>A ENSP00000251595.6:p.Gly60Ser
ENST00000397806.1:c.82G>A ENSP00000380908.1:p.Gly28Ser
ENST00000482565.1:n.314G>A
ENST00000484216.1:n.147G>A
NM_000517.4:c.178G>A NP_000508.1:p.Gly60Ser
NM_000517.6:c.178G>A MANE Select NP_000508.1:p.Gly60Ser
Search 100 bp 5'
Search 100 bp 3'