Canonical Allele Identifier: CA691018154
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1388424497
gnomAD v3: 12-65246109-G-A
gnomAD v4: 12-65246109-G-A
MyVariant Identifiers: chr12:g.65639889G>A (hg19) chr12:g.65246109G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246109G>A , CM000674.2:g.65246109G>A GRCh38
NC_000012.11:g.65639889G>A , CM000674.1:g.65639889G>A GRCh37
NC_000012.10:g.63926156G>A NCBI36
NG_016210.1:g.81539G>A
NG_016210.2:g.81539G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2573-53G>A MANE Select ENSP00000308369.2:n.2573-53G>A
ENST00000308330.2:c.2573-53G>A ENSP00000308369.2:n.2573-53G>A
ENST00000539442.1:n.555-53G>A
ENST00000544506.1:n.293-53G>A
ENST00000545026.1:n.391-53G>A
NM_001167614.1:c.2570-53G>A NP_001161086.1:n.2570-53G>A
NM_014319.4:c.2573-53G>A NP_055134.2:n.2573-53G>A
NM_014319.5:c.2573-53G>A MANE Select NP_055134.2:n.2573-53G>A
NM_001167614.2:c.2570-53G>A NP_001161086.1:n.2570-53G>A
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