Canonical Allele Identifier: CA480743766
Gene: LEMD3 HGNC NCBI

Linked Data

gnomAD v4: 12-65170157-T-A
MyVariant Identifiers: chr12:g.65563937T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170157T>A , CM000674.2:g.65170157T>A GRCh38
NC_000012.11:g.65563937T>A , CM000674.1:g.65563937T>A GRCh37
NC_000012.10:g.63850204T>A NCBI36
NG_016210.1:g.5587T>A
NG_016210.2:g.5587T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.561T>A MANE Select ENSP00000308369.2:p.Ser187=
ENST00000308330.2:c.561T>A ENSP00000308369.2:p.Ser187=
ENST00000541171.1:n.575T>A
NM_001167614.1:c.561T>A NP_001161086.1:p.Ser187=
NM_014319.4:c.561T>A NP_055134.2:p.Ser187=
NM_014319.5:c.561T>A MANE Select NP_055134.2:p.Ser187=
NM_001167614.2:c.561T>A NP_001161086.1:p.Ser187=
Search 100 bp 5'
Search 100 bp 3'