Canonical Allele Identifier: CA163034551
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs538031279
gnomAD v2: 7-97816370-C-G
gnomAD v3: 7-98187058-C-G
gnomAD v4: 7-98187058-C-G
MyVariant Identifiers: chr7:g.97816370C>G (hg19) chr7:g.98187058C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187058C>G , CM000669.2:g.98187058C>G GRCh38
NC_000007.13:g.97816370C>G , CM000669.1:g.97816370C>G GRCh37
NC_000007.12:g.97654306C>G NCBI36
NG_013375.1:g.85174C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297293.6:c.998+60C>G MANE Select ENSP00000297293.5:n.998+60C>G
ENST00000297293.5:c.998+60C>G ENSP00000297293.5:n.998+60C>G
NM_014916.3:c.998+60C>G NP_055731.2:n.998+60C>G
XM_011515981.1:c.992+60C>G XP_011514283.1:n.992+60C>G
XM_011515981.3:c.992+60C>G XP_011514283.1:n.992+60C>G
NM_014916.4:c.998+60C>G MANE Select NP_055731.2:n.998+60C>G
Search 100 bp 5'
Search 100 bp 3'