Canonical Allele Identifier: CA597057533

Gene: LSP1

Linked Data

• dbSNP Id: rs1419066689
• gnomAD v2: 11-1873976-A-C
• gnomAD v3: 11-1852746-A-C
• gnomAD v4: 11-1852746-A-C
• MyVariant Identifiers: chr11:g.1873976A>C (hg19) ; chr11:g.1852746A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1852746A>C , CM000673.2:g.1852746A>C	GRCh38
NC_000011.9:g.1873976A>C , CM000673.1:g.1873976A>C	GRCh37
NC_000011.8:g.1830552A>C	NCBI36
NG_011509.1:g.4777A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000676039.1:c.-192-207A>C	ENSP00000502383.1:n.-192-207A>C