Canonical Allele Identifier: CA2642016450
Gene: LMAN1 HGNC NCBI

Linked Data

gnomAD v4: 18-59359259-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59359259C>T , CM000680.2:g.59359259C>T GRCh38
NC_000018.9:g.57026491C>T , CM000680.1:g.57026491C>T GRCh37
NC_000018.8:g.55177471C>T NCBI36
NG_012097.1:g.5018G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251047.6:c.-15G>A MANE Select ENSP00000251047.4:n.-15G>A
ENST00000251047.5:c.-15G>A ENSP00000251047.4:n.-15G>A
ENST00000587561.1:n.7G>A
NM_005570.3:c.-15G>A NP_005561.1:n.-15G>A
NM_005570.4:c.-15G>A MANE Select NP_005561.1:n.-15G>A
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