Canonical Allele Identifier: CA2200880921
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173512_173513delinsTC , CM000678.2:g.173512_173513delinsTC GRCh38
NC_000016.9:g.223511_223512delinsTC , CM000678.1:g.223511_223512delinsTC GRCh37
NC_000016.8:g.163511_163512delinsTC NCBI36
NG_000006.1:g.34375_34376delinsTC
NG_059186.1:g.1862_1863delinsTC
NG_059271.1:g.5666_5667delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.341_342delinsTC MANE Select ENSP00000251595.6:p.Leu114=
ENST00000251595.10:c.341_342delinsTC ENSP00000251595.6:p.Leu114=
ENST00000397806.1:c.245_246delinsTC ENSP00000380908.1:p.Leu82=
ENST00000482565.1:n.477_478delinsTC
NM_000517.4:c.341_342delinsTC NP_000508.1:p.Leu114=
NM_000517.6:c.341_342delinsTC MANE Select NP_000508.1:p.Leu114=