Canonical Allele Identifier: CA770128172

Gene: ASB3

Linked Data

• dbSNP Id: rs1356443352
• gnomAD v3: 2-53555366-G-A
• gnomAD v4: 2-53555366-G-A
• MyVariant Identifiers: chr2:g.53782503G>A (hg19) ; chr2:g.53555366G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.53555366G>A , CM000664.2:g.53555366G>A	GRCh38
NC_000002.11:g.53782503G>A , CM000664.1:g.53782503G>A	GRCh37
NC_000002.10:g.53636007G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406053.5:c.1436-21482C>T