Canonical Allele Identifier: CA2200880613
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902041626

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173102_173103dup , CM000678.2:g.173102_173103dup GRCh38
NC_000016.9:g.223101_223102dup , CM000678.1:g.223101_223102dup GRCh37
NC_000016.8:g.163101_163102dup NCBI36
NG_000006.1:g.33965_33966dup
NG_059186.1:g.1452_1453dup
NG_059271.1:g.5256_5257dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-23_96-22dup MANE Select ENSP00000251595.6:n.96-23_96-22dup
ENST00000251595.10:c.96-23_96-22dup ENSP00000251595.6:n.96-23_96-22dup
ENST00000397806.1:c.-1-23_-1-22dup ENSP00000380908.1:n.-1-23_-1-22dup
ENST00000482565.1:n.209_210dup
ENST00000484216.1:n.65-23_65-22dup
NM_000517.4:c.96-23_96-22dup NP_000508.1:n.96-23_96-22dup
NM_000517.6:c.96-23_96-22dup MANE Select NP_000508.1:n.96-23_96-22dup