Canonical Allele Identifier: CA718606606
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1182799969
MyVariant Identifiers: chr16:g.223094del (hg19) chr16:g.173095del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173098del , CM000678.2:g.173098del GRCh38
NC_000016.9:g.223097del , CM000678.1:g.223097del GRCh37
NC_000016.8:g.163097del NCBI36
NG_000006.1:g.33961del
NG_059186.1:g.1448del
NG_059271.1:g.5252del

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-27del MANE Select ENSP00000251595.6:n.96-27del
ENST00000251595.10:c.96-27del ENSP00000251595.6:n.96-27del
ENST00000397806.1:c.-1-27del ENSP00000380908.1:n.-1-27del
ENST00000482565.1:n.205del
ENST00000484216.1:n.65-27del
NM_000517.4:c.96-27del NP_000508.1:n.96-27del
NM_000517.6:c.96-27del MANE Select NP_000508.1:n.96-27del
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