Canonical Allele Identifier: CA504061398
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026378C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359146C>T , CM000680.2:g.59359146C>T GRCh38
NC_000018.9:g.57026378C>T , CM000680.1:g.57026378C>T GRCh37
NC_000018.8:g.55177358C>T NCBI36
NG_012097.1:g.5131G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.99G>A MANE Select ENSP00000251047.4:p.Val33=
ENST00000251047.5:c.99G>A ENSP00000251047.4:p.Val33=
ENST00000587561.1:n.120G>A
NM_005570.3:c.99G>A NP_005561.1:p.Val33=
NM_005570.4:c.99G>A MANE Select NP_005561.1:p.Val33=
Search 100 bp 5'
Search 100 bp 3'