Canonical Allele Identifier: CA504061417
Gene: LMAN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.57026402A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359170A>C , CM000680.2:g.59359170A>C GRCh38
NC_000018.9:g.57026402A>C , CM000680.1:g.57026402A>C GRCh37
NC_000018.8:g.55177382A>C NCBI36
NG_012097.1:g.5107T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.75T>G MANE Select ENSP00000251047.4:p.Gly25=
ENST00000251047.5:c.75T>G ENSP00000251047.4:p.Gly25=
ENST00000587561.1:n.96T>G
NM_005570.3:c.75T>G NP_005561.1:p.Gly25=
NM_005570.4:c.75T>G MANE Select NP_005561.1:p.Gly25=
Search 100 bp 5'
Search 100 bp 3'