Canonical Allele Identifier: CA368269954
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797445470
MyVariant Identifiers: chr7:g.97816252G>A (hg19) chr7:g.98186940G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186940G>A , CM000669.2:g.98186940G>A GRCh38
NC_000007.13:g.97816252G>A , CM000669.1:g.97816252G>A GRCh37
NC_000007.12:g.97654188G>A NCBI36
NG_013375.1:g.85056G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.940G>A MANE Select ENSP00000297293.5:p.Val314Ile
ENST00000297293.5:c.940G>A ENSP00000297293.5:p.Val314Ile
NM_014916.3:c.940G>A NP_055731.2:p.Val314Ile
XM_011515981.1:c.934G>A XP_011514283.1:p.Val312Ile
XM_011515981.3:c.934G>A XP_011514283.1:p.Val312Ile
NM_014916.4:c.940G>A MANE Select NP_055731.2:p.Val314Ile
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