Canonical Allele Identifier: CA630396910
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1454049194
gnomAD v2: 18-57026477-C-T
gnomAD v4: 18-59359245-C-T
MyVariant Identifiers: chr18:g.57026477C>T (hg19) chr18:g.59359245C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359245C>T , CM000680.2:g.59359245C>T GRCh38
NC_000018.9:g.57026477C>T , CM000680.1:g.57026477C>T GRCh37
NC_000018.8:g.55177457C>T NCBI36
NG_012097.1:g.5032G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-1G>A MANE Select ENSP00000251047.4:n.-1G>A
ENST00000251047.5:c.-1G>A ENSP00000251047.4:n.-1G>A
ENST00000587561.1:n.21G>A
NM_005570.3:c.-1G>A NP_005561.1:n.-1G>A
NM_005570.4:c.-1G>A MANE Select NP_005561.1:n.-1G>A
Search 100 bp 5'
Search 100 bp 3'