Canonical Allele Identifier: CA2630737135
Gene: HBA2 HGNC NCBI

Linked Data

gnomAD v4: 16-173068-CT-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173069del , CM000678.2:g.173069del GRCh38
NC_000016.9:g.223068del , CM000678.1:g.223068del GRCh37
NC_000016.8:g.163068del NCBI36
NG_000006.1:g.33932del
NG_059186.1:g.1419del
NG_059271.1:g.5223del

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.96-56del MANE Select ENSP00000251595.6:n.96-56del
ENST00000251595.10:c.96-56del ENSP00000251595.6:n.96-56del
ENST00000397806.1:c.-1-56del ENSP00000380908.1:n.-1-56del
ENST00000482565.1:n.176del
ENST00000484216.1:n.65-56del
NM_000517.4:c.96-56del NP_000508.1:n.96-56del
NM_000517.6:c.96-56del MANE Select NP_000508.1:n.96-56del