Canonical Allele Identifier: CA7770196
Gene: HBA2 HGNC NCBI

Linked Data

dbSNP Id: rs755720730
ExAC: 16:223617 C / G
gnomAD v2: 16-223617-C-G
gnomAD v3: 16-173618-C-G
gnomAD v4: 16-173618-C-G
MyVariant Identifiers: chr16:g.223617C>G (hg19) chr16:g.173618C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173618C>G , CM000678.2:g.173618C>G GRCh38
NC_000016.9:g.223617C>G , CM000678.1:g.223617C>G GRCh37
NC_000016.8:g.163617C>G NCBI36
NG_000006.1:g.34481C>G
NG_059186.1:g.1968C>G
NG_059271.1:g.5772C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251595.11:c.*18C>G MANE Select ENSP00000251595.6:n.*18C>G
ENST00000251595.10:c.*18C>G ENSP00000251595.6:n.*18C>G
ENST00000397806.1:c.*18C>G ENSP00000380908.1:n.*18C>G
ENST00000482565.1:n.583C>G
NM_000517.4:c.*18C>G NP_000508.1:n.*18C>G
NM_000517.6:c.*18C>G MANE Select NP_000508.1:n.*18C>G
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