Canonical Allele Identifier: CA919635921

Gene: HBA2

Linked Data

• dbSNP Id: rs1555449365

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173632del , CM000678.2:g.173632del	GRCh38
NC_000016.9:g.223631del , CM000678.1:g.223631del	GRCh37
NC_000016.8:g.163631del	NCBI36
NG_000006.1:g.34495del
NG_059186.1:g.1982del
NG_059271.1:g.5786del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.*32del MANE Select	ENSP00000251595.6:n.*32del
ENST00000251595.10:c.*32del	ENSP00000251595.6:n.*32del
ENST00000397806.1:c.*32del	ENSP00000380908.1:n.*32del
ENST00000482565.1:n.597del
NM_000517.4:c.*32del	NP_000508.1:n.*32del
NM_000517.6:c.*32del MANE Select	NP_000508.1:n.*32del