Canonical Allele Identifier: CA2630737836
Gene: HBA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173448_173450del , CM000678.2:g.173448_173450del GRCh38
NC_000016.9:g.223447_223449del , CM000678.1:g.223447_223449del GRCh37
NC_000016.8:g.163447_163449del NCBI36
NG_000006.1:g.34311_34313del
NG_059186.1:g.1798_1800del
NG_059271.1:g.5602_5604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.301-24_301-22del MANE Select ENSP00000251595.6:n.301-24_301-22del
ENST00000251595.10:c.301-24_301-22del ENSP00000251595.6:n.301-24_301-22del
ENST00000397806.1:c.205-24_205-22del ENSP00000380908.1:n.205-24_205-22del
ENST00000482565.1:n.437-24_437-22del
ENST00000484216.1:n.388_390del
NM_000517.4:c.301-24_301-22del NP_000508.1:n.301-24_301-22del
NM_000517.6:c.301-24_301-22del MANE Select NP_000508.1:n.301-24_301-22del