Canonical Allele Identifier: CA770128014
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs1434378316
MyVariant Identifiers: chr2:g.53782362C>G (hg19) chr2:g.53555225C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555225C>G , CM000664.2:g.53555225C>G GRCh38
NC_000002.11:g.53782362C>G , CM000664.1:g.53782362C>G GRCh37
NC_000002.10:g.53635866C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406053.5:c.1436-21341G>C
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