Canonical Allele Identifier: CA238915755
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1042628112
gnomAD v3: 12-65246420-A-G
gnomAD v4: 12-65246420-A-G
MyVariant Identifiers: chr12:g.65640200A>G (hg19) chr12:g.65246420A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246420A>G , CM000674.2:g.65246420A>G GRCh38
NC_000012.11:g.65640200A>G , CM000674.1:g.65640200A>G GRCh37
NC_000012.10:g.63926467A>G NCBI36
NG_016210.1:g.81850A>G
NG_016210.2:g.81850A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*95A>G MANE Select ENSP00000308369.2:n.*95A>G
ENST00000308330.2:c.*95A>G ENSP00000308369.2:n.*95A>G
ENST00000539442.1:n.813A>G
NM_001167614.1:c.*95A>G NP_001161086.1:n.*95A>G
NM_014319.4:c.*95A>G NP_055134.2:n.*95A>G
NM_014319.5:c.*95A>G MANE Select NP_055134.2:n.*95A>G
NM_001167614.2:c.*95A>G NP_001161086.1:n.*95A>G
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