Canonical Allele Identifier: CA770128139

Gene: ASB3

Linked Data

• dbSNP Id: rs1218410436
• MyVariant Identifiers: chr2:g.53782458_53782459insA (hg19) ; chr2:g.53555321_53555322insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.53555324dup , CM000664.2:g.53555324dup	GRCh38
NC_000002.11:g.53782461dup , CM000664.1:g.53782461dup	GRCh37
NC_000002.10:g.53635965dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406053.5:c.1436-21438dup