Canonical Allele Identifier: CA385671900
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1265523418
gnomAD v2: 12-65633753-T-C
gnomAD v4: 12-65239973-T-C
MyVariant Identifiers: chr12:g.65633753T>C (hg19) chr12:g.65239973T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239973T>C , CM000674.2:g.65239973T>C GRCh38
NC_000012.11:g.65633753T>C , CM000674.1:g.65633753T>C GRCh37
NC_000012.10:g.63920020T>C NCBI36
NG_016210.1:g.75403T>C
NG_016210.2:g.75403T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1966T>C MANE Select ENSP00000308369.2:p.Trp656Arg
ENST00000308330.2:c.1966T>C ENSP00000308369.2:p.Trp656Arg
NM_001167614.1:c.1963T>C NP_001161086.1:p.Trp655Arg
NM_014319.4:c.1966T>C NP_055134.2:p.Trp656Arg
NM_014319.5:c.1966T>C MANE Select NP_055134.2:p.Trp656Arg
NM_001167614.2:c.1963T>C NP_001161086.1:p.Trp655Arg
Search 100 bp 5'
Search 100 bp 3'