Canonical Allele Identifier: CA630396913
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1207763891
gnomAD v2: 18-57026488-G-C
gnomAD v4: 18-59359256-G-C
MyVariant Identifiers: chr18:g.57026488G>C (hg19) chr18:g.59359256G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359256G>C , CM000680.2:g.59359256G>C GRCh38
NC_000018.9:g.57026488G>C , CM000680.1:g.57026488G>C GRCh37
NC_000018.8:g.55177468G>C NCBI36
NG_012097.1:g.5021C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-12C>G MANE Select ENSP00000251047.4:n.-12C>G
ENST00000251047.5:c.-12C>G ENSP00000251047.4:n.-12C>G
ENST00000587561.1:n.10C>G
NM_005570.3:c.-12C>G NP_005561.1:n.-12C>G
NM_005570.4:c.-12C>G MANE Select NP_005561.1:n.-12C>G
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