Canonical Allele Identifier: CA691019077
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1311950398
gnomAD v3: 12-65246964-A-T
gnomAD v4: 12-65246964-A-T
MyVariant Identifiers: chr12:g.65640744A>T (hg19) chr12:g.65246964A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246964A>T , CM000674.2:g.65246964A>T GRCh38
NC_000012.11:g.65640744A>T , CM000674.1:g.65640744A>T GRCh37
NC_000012.10:g.63927011A>T NCBI36
NG_016210.1:g.82394A>T
NG_016210.2:g.82394A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*639A>T MANE Select ENSP00000308369.2:n.*639A>T
ENST00000308330.2:c.*639A>T ENSP00000308369.2:n.*639A>T
NM_001167614.1:c.*639A>T NP_001161086.1:n.*639A>T
NM_014319.4:c.*639A>T NP_055134.2:n.*639A>T
NM_014319.5:c.*639A>T MANE Select NP_055134.2:n.*639A>T
NM_001167614.2:c.*639A>T NP_001161086.1:n.*639A>T
Search 100 bp 5'
Search 100 bp 3'