Canonical Allele Identifier: CA770128177

Gene: ASB3

Linked Data

• dbSNP Id: rs1049710768
• gnomAD v3: 2-53555379-C-G
• gnomAD v4: 2-53555379-C-G
• MyVariant Identifiers: chr2:g.53782516C>G (hg19) ; chr2:g.53555379C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.53555379C>G , CM000664.2:g.53555379C>G	GRCh38
NC_000002.11:g.53782516C>G , CM000664.1:g.53782516C>G	GRCh37
NC_000002.10:g.53636020C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406053.5:c.1436-21495G>C