Canonical Allele Identifier: CA2200880602
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902041269

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173091dup , CM000678.2:g.173091dup GRCh38
NC_000016.9:g.223090dup , CM000678.1:g.223090dup GRCh37
NC_000016.8:g.163090dup NCBI36
NG_000006.1:g.33954dup
NG_059186.1:g.1441dup
NG_059271.1:g.5245dup

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-34dup MANE Select ENSP00000251595.6:n.96-34dup
ENST00000251595.10:c.96-34dup ENSP00000251595.6:n.96-34dup
ENST00000397806.1:c.-1-34dup ENSP00000380908.1:n.-1-34dup
ENST00000482565.1:n.198dup
ENST00000484216.1:n.65-34dup
NM_000517.4:c.96-34dup NP_000508.1:n.96-34dup
NM_000517.6:c.96-34dup MANE Select NP_000508.1:n.96-34dup