Canonical Allele Identifier: CA4355314
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs757267051
ExAC: 7:97816278 A / G
gnomAD v2: 7-97816278-A-G
gnomAD v3: 7-98186966-A-G
gnomAD v4: 7-98186966-A-G
COSMIC: COSM2866014 COSM2866015
MyVariant Identifiers: chr7:g.97816278A>G (hg19) chr7:g.98186966A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186966A>G , CM000669.2:g.98186966A>G GRCh38
NC_000007.13:g.97816278A>G , CM000669.1:g.97816278A>G GRCh37
NC_000007.12:g.97654214A>G NCBI36
NG_013375.1:g.85082A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.966A>G MANE Select ENSP00000297293.5:p.Leu322=
ENST00000297293.5:c.966A>G ENSP00000297293.5:p.Leu322=
NM_014916.3:c.966A>G NP_055731.2:p.Leu322=
XM_011515981.1:c.960A>G XP_011514283.1:p.Leu320=
XM_011515981.3:c.960A>G XP_011514283.1:p.Leu320=
NM_014916.4:c.966A>G MANE Select NP_055731.2:p.Leu322=
Search 100 bp 5'
Search 100 bp 3'