Canonical Allele Identifier: CA1633263637
Gene: LGSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63459629A>G , CM000668.2:g.63459629A>G GRCh38
NC_000006.11:g.64169534A>G , CM000668.1:g.64169534A>G GRCh37
NC_000006.10:g.64227493A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011535890.1:c.-840-15871T>C XP_011534192.1:n.-840-15871T>C
XM_017010929.2:c.-825-15871T>C XP_016866418.1:n.-825-15871T>C