Canonical Allele Identifier: CA47935400
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs866697898
MyVariant Identifiers: chr2:g.53782514C>A (hg19) chr2:g.53555377C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555377C>A , CM000664.2:g.53555377C>A GRCh38
NC_000002.11:g.53782514C>A , CM000664.1:g.53782514C>A GRCh37
NC_000002.10:g.53636018C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406053.5:c.1436-21493G>T
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