Canonical Allele Identifier: CA630396912
Gene: LMAN1 HGNC NCBI

Linked Data

dbSNP Id: rs1401856592
gnomAD v2: 18-57026479-T-G
gnomAD v3: 18-59359247-T-G
gnomAD v4: 18-59359247-T-G
MyVariant Identifiers: chr18:g.57026479T>G (hg19) chr18:g.59359247T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359247T>G , CM000680.2:g.59359247T>G GRCh38
NC_000018.9:g.57026479T>G , CM000680.1:g.57026479T>G GRCh37
NC_000018.8:g.55177459T>G NCBI36
NG_012097.1:g.5030A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-3A>C MANE Select ENSP00000251047.4:n.-3A>C
ENST00000251047.5:c.-3A>C ENSP00000251047.4:n.-3A>C
ENST00000587561.1:n.19A>C
NM_005570.3:c.-3A>C NP_005561.1:n.-3A>C
NM_005570.4:c.-3A>C MANE Select NP_005561.1:n.-3A>C
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