Canonical Allele Identifier: CA238915045
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs926683105
MyVariant Identifiers: chr12:g.65632151A>C (hg19) chr12:g.65238371A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238371A>C , CM000674.2:g.65238371A>C GRCh38
NC_000012.11:g.65632151A>C , CM000674.1:g.65632151A>C GRCh37
NC_000012.10:g.63918418A>C NCBI36
NG_016210.1:g.73801A>C
NG_016210.2:g.73801A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-131A>C MANE Select ENSP00000308369.2:n.1696-131A>C
ENST00000308330.2:c.1696-131A>C ENSP00000308369.2:n.1696-131A>C
NM_001167614.1:c.1693-131A>C NP_001161086.1:n.1693-131A>C
NM_014319.4:c.1696-131A>C NP_055134.2:n.1696-131A>C
NM_014319.5:c.1696-131A>C MANE Select NP_055134.2:n.1696-131A>C
NM_001167614.2:c.1693-131A>C NP_001161086.1:n.1693-131A>C
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