Canonical Allele Identifier: CA163034628
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs991131893
MyVariant Identifiers: chr7:g.97816571C>A (hg19) chr7:g.98187259C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187259C>A , CM000669.2:g.98187259C>A GRCh38
NC_000007.13:g.97816571C>A , CM000669.1:g.97816571C>A GRCh37
NC_000007.12:g.97654507C>A NCBI36
NG_013375.1:g.85375C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+261C>A MANE Select ENSP00000297293.5:n.998+261C>A
ENST00000297293.5:c.998+261C>A ENSP00000297293.5:n.998+261C>A
NM_014916.3:c.998+261C>A NP_055731.2:n.998+261C>A
XM_011515981.1:c.992+261C>A XP_011514283.1:n.992+261C>A
XM_011515981.3:c.992+261C>A XP_011514283.1:n.992+261C>A
NM_014916.4:c.998+261C>A MANE Select NP_055731.2:n.998+261C>A
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