Canonical Allele Identifier: CA480743547
Gene: LEMD3 HGNC NCBI

Linked Data

gnomAD v4: 12-65170100-C-A
MyVariant Identifiers: chr12:g.65563880C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170100C>A , CM000674.2:g.65170100C>A GRCh38
NC_000012.11:g.65563880C>A , CM000674.1:g.65563880C>A GRCh37
NC_000012.10:g.63850147C>A NCBI36
NG_016210.1:g.5530C>A
NG_016210.2:g.5530C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.504C>A MANE Select ENSP00000308369.2:p.Arg168=
ENST00000308330.2:c.504C>A ENSP00000308369.2:p.Arg168=
ENST00000541171.1:n.518C>A
NM_001167614.1:c.504C>A NP_001161086.1:p.Arg168=
NM_014319.4:c.504C>A NP_055134.2:p.Arg168=
NM_014319.5:c.504C>A MANE Select NP_055134.2:p.Arg168=
NM_001167614.2:c.504C>A NP_001161086.1:p.Arg168=
Search 100 bp 5'
Search 100 bp 3'