Canonical Allele Identifier: CA770128183
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs1228521897
MyVariant Identifiers: chr2:g.53782522G>C (hg19) chr2:g.53555385G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555385G>C , CM000664.2:g.53555385G>C GRCh38
NC_000002.11:g.53782522G>C , CM000664.1:g.53782522G>C GRCh37
NC_000002.10:g.53636026G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406053.5:c.1436-21501C>G
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