Canonical Allele Identifier: CA4355294
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs777882880
ExAC: 7:97816142 A / C
MyVariant Identifiers: chr7:g.97816142A>C (hg19) chr7:g.98186830A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186830A>C , CM000669.2:g.98186830A>C GRCh38
NC_000007.13:g.97816142A>C , CM000669.1:g.97816142A>C GRCh37
NC_000007.12:g.97654078A>C NCBI36
NG_013375.1:g.84946A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-47A>C MANE Select ENSP00000297293.5:n.877-47A>C
ENST00000297293.5:c.877-47A>C ENSP00000297293.5:n.877-47A>C
NM_014916.3:c.877-47A>C NP_055731.2:n.877-47A>C
XM_011515981.1:c.871-47A>C XP_011514283.1:n.871-47A>C
XM_011515981.3:c.871-47A>C XP_011514283.1:n.871-47A>C
NM_014916.4:c.877-47A>C MANE Select NP_055731.2:n.877-47A>C
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