Canonical Allele Identifier: CA2200880873
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173447_173448delinsCG , CM000678.2:g.173447_173448delinsCG GRCh38
NC_000016.9:g.223446_223447delinsCG , CM000678.1:g.223446_223447delinsCG GRCh37
NC_000016.8:g.163446_163447delinsCG NCBI36
NG_000006.1:g.34310_34311delinsCG
NG_059186.1:g.1797_1798delinsCG
NG_059271.1:g.5601_5602delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-25_301-24delinsCG MANE Select ENSP00000251595.6:n.301-25_301-24delinsCG
ENST00000251595.10:c.301-25_301-24delinsCG ENSP00000251595.6:n.301-25_301-24delinsCG
ENST00000397806.1:c.205-25_205-24delinsCG ENSP00000380908.1:n.205-25_205-24delinsCG
ENST00000482565.1:n.437-25_437-24delinsCG
ENST00000484216.1:n.387_388delinsCG
NM_000517.4:c.301-25_301-24delinsCG NP_000508.1:n.301-25_301-24delinsCG
NM_000517.6:c.301-25_301-24delinsCG MANE Select NP_000508.1:n.301-25_301-24delinsCG