Canonical Allele Identifier: CA770128077
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs1399590918
gnomAD v3: 2-53555280-C-A
gnomAD v4: 2-53555280-C-A
MyVariant Identifiers: chr2:g.53782417C>A (hg19) chr2:g.53555280C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555280C>A , CM000664.2:g.53555280C>A GRCh38
NC_000002.11:g.53782417C>A , CM000664.1:g.53782417C>A GRCh37
NC_000002.10:g.53635921C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406053.5:c.1436-21396G>T
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