Canonical Allele Identifier: CA480666239
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65633750C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239970C>A , CM000674.2:g.65239970C>A GRCh38
NC_000012.11:g.65633750C>A , CM000674.1:g.65633750C>A GRCh37
NC_000012.10:g.63920017C>A NCBI36
NG_016210.1:g.75400C>A
NG_016210.2:g.75400C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1963C>A MANE Select ENSP00000308369.2:p.Arg655=
ENST00000308330.2:c.1963C>A ENSP00000308369.2:p.Arg655=
NM_001167614.1:c.1960C>A NP_001161086.1:p.Arg654=
NM_014319.4:c.1963C>A NP_055134.2:p.Arg655=
NM_014319.5:c.1963C>A MANE Select NP_055134.2:p.Arg655=
NM_001167614.2:c.1960C>A NP_001161086.1:p.Arg654=