Canonical Allele Identifier: CA368269930
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816246G>C (hg19) chr7:g.98186934G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186934G>C , CM000669.2:g.98186934G>C GRCh38
NC_000007.13:g.97816246G>C , CM000669.1:g.97816246G>C GRCh37
NC_000007.12:g.97654182G>C NCBI36
NG_013375.1:g.85050G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.934G>C MANE Select ENSP00000297293.5:p.Glu312Gln
ENST00000297293.5:c.934G>C ENSP00000297293.5:p.Glu312Gln
NM_014916.3:c.934G>C NP_055731.2:p.Glu312Gln
XM_011515981.1:c.928G>C XP_011514283.1:p.Glu310Gln
XM_011515981.3:c.928G>C XP_011514283.1:p.Glu310Gln
NM_014916.4:c.934G>C MANE Select NP_055731.2:p.Glu312Gln
Search 100 bp 5'
Search 100 bp 3'