Canonical Allele Identifier: CA770128178

Gene: ASB3

Linked Data

• dbSNP Id: rs1400879737
• gnomAD v3: 2-53555381-A-C
• gnomAD v4: 2-53555381-A-C
• MyVariant Identifiers: chr2:g.53782518A>C (hg19) ; chr2:g.53555381A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.53555381A>C , CM000664.2:g.53555381A>C	GRCh38
NC_000002.11:g.53782518A>C , CM000664.1:g.53782518A>C	GRCh37
NC_000002.10:g.53636022A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406053.5:c.1436-21497T>G