Canonical Allele Identifier: CA301006659
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1034602687
gnomAD v4: 18-59359261-C-T
MyVariant Identifiers: chr18:g.59359261C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359261C>T , CM000680.2:g.59359261C>T GRCh38
NC_000018.9:g.57026493C>T , CM000680.1:g.57026493C>T GRCh37
NC_000018.8:g.55177473C>T NCBI36
NG_012097.1:g.5016G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-17G>A MANE Select ENSP00000251047.4:n.-17G>A
ENST00000251047.5:c.-17G>A ENSP00000251047.4:n.-17G>A
ENST00000587561.1:n.5G>A
NM_005570.3:c.-17G>A NP_005561.1:n.-17G>A
NM_005570.4:c.-17G>A MANE Select NP_005561.1:n.-17G>A
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