Canonical Allele Identifier: CA480669708
Gene: LEMD3 HGNC NCBI

Linked Data

gnomAD v4: 12-65246295-T-C
MyVariant Identifiers: chr12:g.65640075T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246295T>C , CM000674.2:g.65246295T>C GRCh38
NC_000012.11:g.65640075T>C , CM000674.1:g.65640075T>C GRCh37
NC_000012.10:g.63926342T>C NCBI36
NG_016210.1:g.81725T>C
NG_016210.2:g.81725T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2706T>C MANE Select ENSP00000308369.2:p.Thr902=
ENST00000308330.2:c.2706T>C ENSP00000308369.2:p.Thr902=
ENST00000539442.1:n.688T>C
ENST00000545026.1:n.524T>C
NM_001167614.1:c.2703T>C NP_001161086.1:p.Thr901=
NM_014319.4:c.2706T>C NP_055134.2:p.Thr902=
NM_014319.5:c.2706T>C MANE Select NP_055134.2:p.Thr902=
NM_001167614.2:c.2703T>C NP_001161086.1:p.Thr901=
Search 100 bp 5'
Search 100 bp 3'