Canonical Allele Identifier: CA480669839
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65640099T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246319T>C , CM000674.2:g.65246319T>C GRCh38
NC_000012.11:g.65640099T>C , CM000674.1:g.65640099T>C GRCh37
NC_000012.10:g.63926366T>C NCBI36
NG_016210.1:g.81749T>C
NG_016210.2:g.81749T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2730T>C MANE Select ENSP00000308369.2:p.Ser910=
ENST00000308330.2:c.2730T>C ENSP00000308369.2:p.Ser910=
ENST00000539442.1:n.712T>C
ENST00000545026.1:n.548T>C
NM_001167614.1:c.2727T>C NP_001161086.1:p.Ser909=
NM_014319.4:c.2730T>C NP_055134.2:p.Ser910=
NM_014319.5:c.2730T>C MANE Select NP_055134.2:p.Ser910=
NM_001167614.2:c.2727T>C NP_001161086.1:p.Ser909=
Search 100 bp 5'
Search 100 bp 3'