Canonical Allele Identifier: CA2042444160
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1592462116

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238476T>G , CM000674.2:g.65238476T>G GRCh38
NC_000012.11:g.65632256T>G , CM000674.1:g.65632256T>G GRCh37
NC_000012.10:g.63918523T>G NCBI36
NG_016210.1:g.73906T>G
NG_016210.2:g.73906T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1696-26T>G MANE Select ENSP00000308369.2:n.1696-26T>G
ENST00000308330.2:c.1696-26T>G ENSP00000308369.2:n.1696-26T>G
NM_001167614.1:c.1693-26T>G NP_001161086.1:n.1693-26T>G
NM_014319.4:c.1696-26T>G NP_055134.2:n.1696-26T>G
NM_014319.5:c.1696-26T>G MANE Select NP_055134.2:n.1696-26T>G
NM_001167614.2:c.1693-26T>G NP_001161086.1:n.1693-26T>G