Canonical Allele Identifier: CA691027696
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1449473687
gnomAD v3: 12-65238428-G-A
gnomAD v4: 12-65238428-G-A
MyVariant Identifiers: chr12:g.65632208G>A (hg19) chr12:g.65238428G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238428G>A , CM000674.2:g.65238428G>A GRCh38
NC_000012.11:g.65632208G>A , CM000674.1:g.65632208G>A GRCh37
NC_000012.10:g.63918475G>A NCBI36
NG_016210.1:g.73858G>A
NG_016210.2:g.73858G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-74G>A MANE Select ENSP00000308369.2:n.1696-74G>A
ENST00000308330.2:c.1696-74G>A ENSP00000308369.2:n.1696-74G>A
NM_001167614.1:c.1693-74G>A NP_001161086.1:n.1693-74G>A
NM_014319.4:c.1696-74G>A NP_055134.2:n.1696-74G>A
NM_014319.5:c.1696-74G>A MANE Select NP_055134.2:n.1696-74G>A
NM_001167614.2:c.1693-74G>A NP_001161086.1:n.1693-74G>A
Search 100 bp 5'
Search 100 bp 3'