Canonical Allele Identifier: CA216187387
Gene: LSP1 HGNC NCBI

Linked Data

dbSNP Id: rs926466588
MyVariant Identifiers: chr11:g.1874013C>T (hg19) chr11:g.1852783C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852783C>T , CM000673.2:g.1852783C>T GRCh38
NC_000011.9:g.1874013C>T , CM000673.1:g.1874013C>T GRCh37
NC_000011.8:g.1830589C>T NCBI36
NG_011509.1:g.4814C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-170C>T ENSP00000502383.1:n.-192-170C>T
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