Canonical Allele Identifier: CA6671048
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs748299191
ExAC: 12:65632487 T / C
gnomAD v2: 12-65632487-T-C
gnomAD v4: 12-65238707-T-C
MyVariant Identifiers: chr12:g.65632487T>C (hg19) chr12:g.65238707T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238707T>C , CM000674.2:g.65238707T>C GRCh38
NC_000012.11:g.65632487T>C , CM000674.1:g.65632487T>C GRCh37
NC_000012.10:g.63918754T>C NCBI36
NG_016210.1:g.74137T>C
NG_016210.2:g.74137T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1814T>C MANE Select ENSP00000308369.2:p.Ile605Thr
ENST00000308330.2:c.1814T>C ENSP00000308369.2:p.Ile605Thr
NM_001167614.1:c.1811T>C NP_001161086.1:p.Ile604Thr
NM_014319.4:c.1814T>C NP_055134.2:p.Ile605Thr
NM_014319.5:c.1814T>C MANE Select NP_055134.2:p.Ile605Thr
NM_001167614.2:c.1811T>C NP_001161086.1:p.Ile604Thr
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