Canonical Allele Identifier: CA402595759
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1346522200
gnomAD v4: 18-59359150-C-T
MyVariant Identifiers: chr18:g.57026382C>T (hg19) chr18:g.59359150C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359150C>T , CM000680.2:g.59359150C>T GRCh38
NC_000018.9:g.57026382C>T , CM000680.1:g.57026382C>T GRCh37
NC_000018.8:g.55177362C>T NCBI36
NG_012097.1:g.5127G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.95G>A MANE Select ENSP00000251047.4:p.Gly32Asp
ENST00000251047.5:c.95G>A ENSP00000251047.4:p.Gly32Asp
ENST00000587561.1:n.116G>A
NM_005570.3:c.95G>A NP_005561.1:p.Gly32Asp
NM_005570.4:c.95G>A MANE Select NP_005561.1:p.Gly32Asp
Search 100 bp 5'
Search 100 bp 3'