Canonical Allele Identifier: CA770128155
Gene: ASB3 HGNC NCBI

Linked Data

dbSNP Id: rs1282193672
MyVariant Identifiers: chr2:g.53782473A>C (hg19) chr2:g.53555336A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53555336A>C , CM000664.2:g.53555336A>C GRCh38
NC_000002.11:g.53782473A>C , CM000664.1:g.53782473A>C GRCh37
NC_000002.10:g.53635977A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406053.5:c.1436-21452T>G
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