Canonical Allele Identifier: CA163034617
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1054814693
MyVariant Identifiers: chr7:g.97816492T>A (hg19) chr7:g.98187180T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187180T>A , CM000669.2:g.98187180T>A GRCh38
NC_000007.13:g.97816492T>A , CM000669.1:g.97816492T>A GRCh37
NC_000007.12:g.97654428T>A NCBI36
NG_013375.1:g.85296T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+182T>A MANE Select ENSP00000297293.5:n.998+182T>A
ENST00000297293.5:c.998+182T>A ENSP00000297293.5:n.998+182T>A
NM_014916.3:c.998+182T>A NP_055731.2:n.998+182T>A
XM_011515981.1:c.992+182T>A XP_011514283.1:n.992+182T>A
XM_011515981.3:c.992+182T>A XP_011514283.1:n.992+182T>A
NM_014916.4:c.998+182T>A MANE Select NP_055731.2:n.998+182T>A
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