Canonical Allele Identifier: CA402595762
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs368204045
MyVariant Identifiers: chr18:g.57026383C>T (hg19) chr18:g.59359151C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359151C>T , CM000680.2:g.59359151C>T GRCh38
NC_000018.9:g.57026383C>T , CM000680.1:g.57026383C>T GRCh37
NC_000018.8:g.55177363C>T NCBI36
NG_012097.1:g.5126G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.94G>A MANE Select ENSP00000251047.4:p.Gly32Ser
ENST00000251047.5:c.94G>A ENSP00000251047.4:p.Gly32Ser
ENST00000587561.1:n.115G>A
NM_005570.3:c.94G>A NP_005561.1:p.Gly32Ser
NM_005570.4:c.94G>A MANE Select NP_005561.1:p.Gly32Ser
Search 100 bp 5'
Search 100 bp 3'