Canonical Allele Identifier: CA2200880990
Gene: HBA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173600_173601delinsAG , CM000678.2:g.173600_173601delinsAG GRCh38
NC_000016.9:g.223599_223600delinsAG , CM000678.1:g.223599_223600delinsAG GRCh37
NC_000016.8:g.163599_163600delinsAG NCBI36
NG_000006.1:g.34463_34464delinsAG
NG_059186.1:g.1950_1951delinsAG
NG_059271.1:g.5754_5755delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000251595.11:c.429_*1delinsAG MANE Select ENSP00000251595.6:n.[c.429_*1delinsAG;Ter...
ENST00000251595.10:c.429_*1delinsAG ENSP00000251595.6:n.[c.429_*1delinsAG;Ter...
ENST00000397806.1:c.333_*1delinsAG ENSP00000380908.1:n.[c.333_*1delinsAG;Ter...
ENST00000482565.1:n.565_566delinsAG
NM_000517.4:c.429_*1delinsAG NP_000508.1:n.[c.429_*1delinsAG;Ter143=]
NM_000517.6:c.429_*1delinsAG MANE Select NP_000508.1:n.[c.429_*1delinsAG;Ter143=]