Canonical Allele Identifier: CA368270314
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816307T>C (hg19) chr7:g.98186995T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186995T>C , CM000669.2:g.98186995T>C GRCh38
NC_000007.13:g.97816307T>C , CM000669.1:g.97816307T>C GRCh37
NC_000007.12:g.97654243T>C NCBI36
NG_013375.1:g.85111T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.995T>C MANE Select ENSP00000297293.5:p.Ile332Thr
ENST00000297293.5:c.995T>C ENSP00000297293.5:p.Ile332Thr
NM_014916.3:c.995T>C NP_055731.2:p.Ile332Thr
XM_011515981.1:c.989T>C XP_011514283.1:p.Ile330Thr
XM_011515981.3:c.989T>C XP_011514283.1:p.Ile330Thr
NM_014916.4:c.995T>C MANE Select NP_055731.2:p.Ile332Thr
Search 100 bp 5'
Search 100 bp 3'