Canonical Allele Identifier: CA402595754
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026379A>T (hg19) chr18:g.59359147A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359147A>T , CM000680.2:g.59359147A>T GRCh38
NC_000018.9:g.57026379A>T , CM000680.1:g.57026379A>T GRCh37
NC_000018.8:g.55177359A>T NCBI36
NG_012097.1:g.5130T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.98T>A MANE Select ENSP00000251047.4:p.Val33Glu
ENST00000251047.5:c.98T>A ENSP00000251047.4:p.Val33Glu
ENST00000587561.1:n.119T>A
NM_005570.3:c.98T>A NP_005561.1:p.Val33Glu
NM_005570.4:c.98T>A MANE Select NP_005561.1:p.Val33Glu
Search 100 bp 5'
Search 100 bp 3'