Canonical Allele Identifier: CA216187469
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs538809649
gnomAD v3: 11-1852864-G-C
gnomAD v4: 11-1852864-G-C
MyVariant Identifiers: chr11:g.1874094G>C (hg19) chr11:g.1852864G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852864G>C , CM000673.2:g.1852864G>C GRCh38
NC_000011.9:g.1874094G>C , CM000673.1:g.1874094G>C GRCh37
NC_000011.8:g.1830670G>C NCBI36
NG_011509.1:g.4895G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-89G>C ENSP00000502383.1:n.-192-89G>C
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