Canonical Allele Identifier: CA480666179
Gene: LEMD3 HGNC NCBI

Linked Data

gnomAD v4: 12-65238783-T-A
MyVariant Identifiers: chr12:g.65632563T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238783T>A , CM000674.2:g.65238783T>A GRCh38
NC_000012.11:g.65632563T>A , CM000674.1:g.65632563T>A GRCh37
NC_000012.10:g.63918830T>A NCBI36
NG_016210.1:g.74213T>A
NG_016210.2:g.74213T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1890T>A MANE Select ENSP00000308369.2:p.Thr630=
ENST00000308330.2:c.1890T>A ENSP00000308369.2:p.Thr630=
NM_001167614.1:c.1887T>A NP_001161086.1:p.Thr629=
NM_014319.4:c.1890T>A NP_055134.2:p.Thr630=
NM_014319.5:c.1890T>A MANE Select NP_055134.2:p.Thr630=
NM_001167614.2:c.1887T>A NP_001161086.1:p.Thr629=
Search 100 bp 5'
Search 100 bp 3'