Canonical Allele Identifier: CA566354575
Gene: LST1 HGNC NCBI

Linked Data

dbSNP Id: rs17200775
gnomAD v2: 6-31553936-G-T
gnomAD v4: 6-31586159-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31586159G>T , CM000668.2:g.31586159G>T GRCh38
NC_000006.11:g.31553936G>T , CM000668.1:g.31553936G>T GRCh37
NC_000006.10:g.31661915G>T NCBI36
NG_030378.1:g.4981G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000418507.6:c.-257G>T ENSP00000405900.2:n.-257G>T