Canonical Allele Identifier: CA368270068
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1562918602
gnomAD v4: 7-98186967-A-C
MyVariant Identifiers: chr7:g.97816279A>C (hg19) chr7:g.98186967A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186967A>C , CM000669.2:g.98186967A>C GRCh38
NC_000007.13:g.97816279A>C , CM000669.1:g.97816279A>C GRCh37
NC_000007.12:g.97654215A>C NCBI36
NG_013375.1:g.85083A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.967A>C MANE Select ENSP00000297293.5:p.Thr323Pro
ENST00000297293.5:c.967A>C ENSP00000297293.5:p.Thr323Pro
NM_014916.3:c.967A>C NP_055731.2:p.Thr323Pro
XM_011515981.1:c.961A>C XP_011514283.1:p.Thr321Pro
XM_011515981.3:c.961A>C XP_011514283.1:p.Thr321Pro
NM_014916.4:c.967A>C MANE Select NP_055731.2:p.Thr323Pro
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