Canonical Allele Identifier: CA2630737726
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173338-CG-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173341del , CM000678.2:g.173341del GRCh38
NC_000016.9:g.223340del , CM000678.1:g.223340del GRCh37
NC_000016.8:g.163340del NCBI36
NG_000006.1:g.34204del
NG_059186.1:g.1691del
NG_059271.1:g.5495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.300+12del MANE Select ENSP00000251595.6:n.300+12del
ENST00000251595.10:c.300+12del ENSP00000251595.6:n.300+12del
ENST00000397806.1:c.204+12del ENSP00000380908.1:n.204+12del
ENST00000482565.1:n.436+12del
ENST00000484216.1:n.281del
NM_000517.4:c.300+12del NP_000508.1:n.300+12del
NM_000517.6:c.300+12del MANE Select NP_000508.1:n.300+12del