Canonical Allele Identifier: CA238915046
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs780508446
gnomAD v3: 12-65238380-A-G
gnomAD v4: 12-65238380-A-G
MyVariant Identifiers: chr12:g.65632160A>G (hg19) chr12:g.65238380A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238380A>G , CM000674.2:g.65238380A>G GRCh38
NC_000012.11:g.65632160A>G , CM000674.1:g.65632160A>G GRCh37
NC_000012.10:g.63918427A>G NCBI36
NG_016210.1:g.73810A>G
NG_016210.2:g.73810A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-122A>G MANE Select ENSP00000308369.2:n.1696-122A>G
ENST00000308330.2:c.1696-122A>G ENSP00000308369.2:n.1696-122A>G
NM_001167614.1:c.1693-122A>G NP_001161086.1:n.1693-122A>G
NM_014319.4:c.1696-122A>G NP_055134.2:n.1696-122A>G
NM_014319.5:c.1696-122A>G MANE Select NP_055134.2:n.1696-122A>G
NM_001167614.2:c.1693-122A>G NP_001161086.1:n.1693-122A>G
Search 100 bp 5'
Search 100 bp 3'