Canonical Allele Identifier: CA385671148
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65632490C>G (hg19) chr12:g.65238710C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238710C>G , CM000674.2:g.65238710C>G GRCh38
NC_000012.11:g.65632490C>G , CM000674.1:g.65632490C>G GRCh37
NC_000012.10:g.63918757C>G NCBI36
NG_016210.1:g.74140C>G
NG_016210.2:g.74140C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1817C>G MANE Select ENSP00000308369.2:p.Thr606Ser
ENST00000308330.2:c.1817C>G ENSP00000308369.2:p.Thr606Ser
NM_001167614.1:c.1814C>G NP_001161086.1:p.Thr605Ser
NM_014319.4:c.1817C>G NP_055134.2:p.Thr606Ser
NM_014319.5:c.1817C>G MANE Select NP_055134.2:p.Thr606Ser
NM_001167614.2:c.1814C>G NP_001161086.1:p.Thr605Ser
Search 100 bp 5'
Search 100 bp 3'