Canonical Allele Identifier: CA844372543
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1419211841
gnomAD v3: 7-98187200-C-T
gnomAD v4: 7-98187200-C-T
MyVariant Identifiers: chr7:g.97816512C>T (hg19) chr7:g.98187200C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187200C>T , CM000669.2:g.98187200C>T GRCh38
NC_000007.13:g.97816512C>T , CM000669.1:g.97816512C>T GRCh37
NC_000007.12:g.97654448C>T NCBI36
NG_013375.1:g.85316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+202C>T MANE Select ENSP00000297293.5:n.998+202C>T
ENST00000297293.5:c.998+202C>T ENSP00000297293.5:n.998+202C>T
NM_014916.3:c.998+202C>T NP_055731.2:n.998+202C>T
XM_011515981.1:c.992+202C>T XP_011514283.1:n.992+202C>T
XM_011515981.3:c.992+202C>T XP_011514283.1:n.992+202C>T
NM_014916.4:c.998+202C>T MANE Select NP_055731.2:n.998+202C>T
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