Canonical Allele Identifier: CA368270344
Gene: LMTK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.97816310G>C (hg19) chr7:g.98186998G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186998G>C , CM000669.2:g.98186998G>C GRCh38
NC_000007.13:g.97816310G>C , CM000669.1:g.97816310G>C GRCh37
NC_000007.12:g.97654246G>C NCBI36
NG_013375.1:g.85114G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998G>C MANE Select ENSP00000297293.5:p.Trp333Ser
ENST00000297293.5:c.998G>C ENSP00000297293.5:p.Trp333Ser
NM_014916.3:c.998G>C NP_055731.2:p.Trp333Ser
XM_011515981.1:c.992G>C XP_011514283.1:p.Trp331Ser
XM_011515981.3:c.992G>C XP_011514283.1:p.Trp331Ser
NM_014916.4:c.998G>C MANE Select NP_055731.2:p.Trp333Ser
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