Canonical Allele Identifier: CA47935374
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs926533799
gnomAD v3: 2-53555272-T-C
gnomAD v4: 2-53555272-T-C
MyVariant Identifiers: chr2:g.53782409T>C (hg19) chr2:g.53555272T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555272T>C , CM000664.2:g.53555272T>C GRCh38
NC_000002.11:g.53782409T>C , CM000664.1:g.53782409T>C GRCh37
NC_000002.10:g.53635913T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406053.5:c.1436-21388A>G
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