Canonical Allele Identifier: CA456635325
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816272A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186960A>G , CM000669.2:g.98186960A>G GRCh38
NC_000007.13:g.97816272A>G , CM000669.1:g.97816272A>G GRCh37
NC_000007.12:g.97654208A>G NCBI36
NG_013375.1:g.85076A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.960A>G MANE Select ENSP00000297293.5:p.Arg320=
ENST00000297293.5:c.960A>G ENSP00000297293.5:p.Arg320=
NM_014916.3:c.960A>G NP_055731.2:p.Arg320=
XM_011515981.1:c.954A>G XP_011514283.1:p.Arg318=
XM_011515981.3:c.954A>G XP_011514283.1:p.Arg318=
NM_014916.4:c.960A>G MANE Select NP_055731.2:p.Arg320=