Canonical Allele Identifier: CA504061409
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs768277376
gnomAD v2: 18-57026392-G-T
gnomAD v4: 18-59359160-G-T
MyVariant Identifiers: chr18:g.57026392G>T (hg19) chr18:g.59359160G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359160G>T , CM000680.2:g.59359160G>T GRCh38
NC_000018.9:g.57026392G>T , CM000680.1:g.57026392G>T GRCh37
NC_000018.8:g.55177372G>T NCBI36
NG_012097.1:g.5117C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251047.6:c.85C>A MANE Select ENSP00000251047.4:p.Arg29=
ENST00000251047.5:c.85C>A ENSP00000251047.4:p.Arg29=
ENST00000587561.1:n.106C>A
NM_005570.3:c.85C>A NP_005561.1:p.Arg29=
NM_005570.4:c.85C>A MANE Select NP_005561.1:p.Arg29=
Search 100 bp 5'
Search 100 bp 3'