Canonical Allele Identifier: CA973581897
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs1902041579
gnomAD v3: 16-173099-A-C
gnomAD v4: 16-173099-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173099A>C , CM000678.2:g.173099A>C GRCh38
NC_000016.9:g.223098A>C , CM000678.1:g.223098A>C GRCh37
NC_000016.8:g.163098A>C NCBI36
NG_000006.1:g.33962A>C
NG_059186.1:g.1449A>C
NG_059271.1:g.5253A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.96-26A>C MANE Select ENSP00000251595.6:n.96-26A>C
ENST00000251595.10:c.96-26A>C ENSP00000251595.6:n.96-26A>C
ENST00000397806.1:c.-1-26A>C ENSP00000380908.1:n.-1-26A>C
ENST00000482565.1:n.206A>C
ENST00000484216.1:n.65-26A>C
NM_000517.4:c.96-26A>C NP_000508.1:n.96-26A>C
NM_000517.6:c.96-26A>C MANE Select NP_000508.1:n.96-26A>C
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