Canonical Allele Identifier: CA238915795
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs547604504
gnomAD v3: 12-65246917-G-C
gnomAD v4: 12-65246917-G-C
MyVariant Identifiers: chr12:g.65640697G>C (hg19) chr12:g.65246917G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246917G>C , CM000674.2:g.65246917G>C GRCh38
NC_000012.11:g.65640697G>C , CM000674.1:g.65640697G>C GRCh37
NC_000012.10:g.63926964G>C NCBI36
NG_016210.1:g.82347G>C
NG_016210.2:g.82347G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*592G>C MANE Select ENSP00000308369.2:n.*592G>C
ENST00000308330.2:c.*592G>C ENSP00000308369.2:n.*592G>C
NM_001167614.1:c.*592G>C NP_001161086.1:n.*592G>C
NM_014319.4:c.*592G>C NP_055134.2:n.*592G>C
NM_014319.5:c.*592G>C MANE Select NP_055134.2:n.*592G>C
NM_001167614.2:c.*592G>C NP_001161086.1:n.*592G>C
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