Canonical Allele Identifier: CA915946211
Gene: HBA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 811183
dbSNP Id: rs1596570272

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173448delinsCTCGGCCC , CM000678.2:g.173448delinsCTCGGCCC GRCh38
NC_000016.9:g.223447delinsCTCGGCCC , CM000678.1:g.223447delinsCTCGGCCC GRCh37
NC_000016.8:g.163447delinsCTCGGCCC NCBI36
NG_000006.1:g.34311delinsCTCGGCCC
NG_059186.1:g.1798delinsCTCGGCCC
NG_059271.1:g.5602delinsCTCGGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-24delinsCTCGGCCC MANE Select ENSP00000251595.6:n.301-24delinsCTCGGCCC
ENST00000251595.10:c.301-24delinsCTCGGCCC ENSP00000251595.6:n.301-24delinsCTCGGCCC
ENST00000397806.1:c.205-24delinsCTCGGCCC ENSP00000380908.1:n.205-24delinsCTCGGCCC
ENST00000482565.1:n.437-24delinsCTCGGCCC
ENST00000484216.1:n.388delinsCTCGGCCC
NM_000517.4:c.301-24delinsCTCGGCCC NP_000508.1:n.301-24delinsCTCGGCCC
NM_000517.6:c.301-24delinsCTCGGCCC MANE Select NP_000508.1:n.301-24delinsCTCGGCCC