Canonical Allele Identifier: CA385670879
Gene: LEMD3 HGNC NCBI

Linked Data

gnomAD v4: 12-65238508-G-A
MyVariant Identifiers: chr12:g.65632288G>A (hg19) chr12:g.65238508G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238508G>A , CM000674.2:g.65238508G>A GRCh38
NC_000012.11:g.65632288G>A , CM000674.1:g.65632288G>A GRCh37
NC_000012.10:g.63918555G>A NCBI36
NG_016210.1:g.73938G>A
NG_016210.2:g.73938G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1702G>A MANE Select ENSP00000308369.2:p.Gly568Ser
ENST00000308330.2:c.1702G>A ENSP00000308369.2:p.Gly568Ser
NM_001167614.1:c.1699G>A NP_001161086.1:p.Gly567Ser
NM_014319.4:c.1702G>A NP_055134.2:p.Gly568Ser
NM_014319.5:c.1702G>A MANE Select NP_055134.2:p.Gly568Ser
NM_001167614.2:c.1699G>A NP_001161086.1:p.Gly567Ser
Search 100 bp 5'
Search 100 bp 3'