Canonical Allele Identifier: CA480666124
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65632476A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238696A>G , CM000674.2:g.65238696A>G GRCh38
NC_000012.11:g.65632476A>G , CM000674.1:g.65632476A>G GRCh37
NC_000012.10:g.63918743A>G NCBI36
NG_016210.1:g.74126A>G
NG_016210.2:g.74126A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1803A>G MANE Select ENSP00000308369.2:p.Glu601=
ENST00000308330.2:c.1803A>G ENSP00000308369.2:p.Glu601=
NM_001167614.1:c.1800A>G NP_001161086.1:p.Glu600=
NM_014319.4:c.1803A>G NP_055134.2:p.Glu601=
NM_014319.5:c.1803A>G MANE Select NP_055134.2:p.Glu601=
NM_001167614.2:c.1800A>G NP_001161086.1:p.Glu600=
Search 100 bp 5'
Search 100 bp 3'