Canonical Allele Identifier: CA630396916
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1245631968
gnomAD v2: 18-57026494-G-C
gnomAD v4: 18-59359262-G-C
MyVariant Identifiers: chr18:g.57026494G>C (hg19) chr18:g.59359262G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359262G>C , CM000680.2:g.59359262G>C GRCh38
NC_000018.9:g.57026494G>C , CM000680.1:g.57026494G>C GRCh37
NC_000018.8:g.55177474G>C NCBI36
NG_012097.1:g.5015C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-18C>G MANE Select ENSP00000251047.4:n.-18C>G
ENST00000251047.5:c.-18C>G ENSP00000251047.4:n.-18C>G
ENST00000587561.1:n.4C>G
NM_005570.3:c.-18C>G NP_005561.1:n.-18C>G
NM_005570.4:c.-18C>G MANE Select NP_005561.1:n.-18C>G
Search 100 bp 5'
Search 100 bp 3'