Canonical Allele Identifier: CA402595783
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026394A>T (hg19) chr18:g.59359162A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359162A>T , CM000680.2:g.59359162A>T GRCh38
NC_000018.9:g.57026394A>T , CM000680.1:g.57026394A>T GRCh37
NC_000018.8:g.55177374A>T NCBI36
NG_012097.1:g.5115T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.83T>A MANE Select ENSP00000251047.4:p.Val28Asp
ENST00000251047.5:c.83T>A ENSP00000251047.4:p.Val28Asp
ENST00000587561.1:n.104T>A
NM_005570.3:c.83T>A NP_005561.1:p.Val28Asp
NM_005570.4:c.83T>A MANE Select NP_005561.1:p.Val28Asp
Search 100 bp 5'
Search 100 bp 3'