Canonical Allele Identifier: CA770128134

Gene: ASB3

Linked Data

• dbSNP Id: rs930197418
• MyVariant Identifiers: chr2:g.53782437G>T (hg19) ; chr2:g.53555300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.53555300G>T , CM000664.2:g.53555300G>T	GRCh38
NC_000002.11:g.53782437G>T , CM000664.1:g.53782437G>T	GRCh37
NC_000002.10:g.53635941G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406053.5:c.1436-21416C>A