Canonical Allele Identifier: CA163034380
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs111998978
gnomAD v2: 7-97816072-T-C
gnomAD v3: 7-98186760-T-C
gnomAD v4: 7-98186760-T-C
MyVariant Identifiers: chr7:g.97816072T>C (hg19) chr7:g.98186760T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186760T>C , CM000669.2:g.98186760T>C GRCh38
NC_000007.13:g.97816072T>C , CM000669.1:g.97816072T>C GRCh37
NC_000007.12:g.97654008T>C NCBI36
NG_013375.1:g.84876T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-117T>C MANE Select ENSP00000297293.5:n.877-117T>C
ENST00000297293.5:c.877-117T>C ENSP00000297293.5:n.877-117T>C
NM_014916.3:c.877-117T>C NP_055731.2:n.877-117T>C
XM_011515981.1:c.871-117T>C XP_011514283.1:n.871-117T>C
XM_011515981.3:c.871-117T>C XP_011514283.1:n.871-117T>C
NM_014916.4:c.877-117T>C MANE Select NP_055731.2:n.877-117T>C
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