Canonical Allele Identifier: CA6670712
Gene: LEMD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 310219
ClinVar RCV Id: RCV001513962
dbSNP Id: rs61736594
ExAC: 12:65563712 C / T
gnomAD v2: 12-65563712-C-T
gnomAD v3: 12-65169932-C-T
gnomAD v4: 12-65169932-C-T
MyVariant Identifiers: chr12:g.65563712C>T (hg19) chr12:g.65169932C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65169932C>T , CM000674.2:g.65169932C>T GRCh38
NC_000012.11:g.65563712C>T , CM000674.1:g.65563712C>T GRCh37
NC_000012.10:g.63849979C>T NCBI36
NG_016210.1:g.5362C>T
NG_016210.2:g.5362C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.336C>T MANE Select ENSP00000308369.2:p.Ala112=
ENST00000308330.2:c.336C>T ENSP00000308369.2:p.Ala112=
ENST00000541171.1:n.350C>T
NM_001167614.1:c.336C>T NP_001161086.1:p.Ala112=
NM_014319.4:c.336C>T NP_055134.2:p.Ala112=
NM_014319.5:c.336C>T MANE Select NP_055134.2:p.Ala112=
NM_001167614.2:c.336C>T NP_001161086.1:p.Ala112=
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