Canonical Allele Identifier: CA2832338615
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.172880T>C , CM000678.2:g.172880T>C GRCh38
NC_000016.9:g.222879T>C , CM000678.1:g.222879T>C GRCh37
NC_000016.8:g.162879T>C NCBI36
NG_000006.1:g.33743T>C
NG_059186.1:g.1230T>C
NG_059271.1:g.5034T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.-33T>C MANE Select ENSP00000251595.6:n.-33T>C
ENST00000251595.10:c.-33T>C ENSP00000251595.6:n.-33T>C
NM_000517.4:c.-33T>C NP_000508.1:n.-33T>C
NM_000517.6:c.-33T>C MANE Select NP_000508.1:n.-33T>C