Canonical Allele Identifier: CA163034642
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs971102973
MyVariant Identifiers: chr7:g.97816592T>C (hg19) chr7:g.98187280T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187280T>C , CM000669.2:g.98187280T>C GRCh38
NC_000007.13:g.97816592T>C , CM000669.1:g.97816592T>C GRCh37
NC_000007.12:g.97654528T>C NCBI36
NG_013375.1:g.85396T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+282T>C MANE Select ENSP00000297293.5:n.998+282T>C
ENST00000297293.5:c.998+282T>C ENSP00000297293.5:n.998+282T>C
NM_014916.3:c.998+282T>C NP_055731.2:n.998+282T>C
XM_011515981.1:c.992+282T>C XP_011514283.1:n.992+282T>C
XM_011515981.3:c.992+282T>C XP_011514283.1:n.992+282T>C
NM_014916.4:c.998+282T>C MANE Select NP_055731.2:n.998+282T>C
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