Canonical Allele Identifier: CA1728472168
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1797446725
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98187055C>G , CM000669.2:g.98187055C>G GRCh38
NC_000007.13:g.97816367C>G , CM000669.1:g.97816367C>G GRCh37
NC_000007.12:g.97654303C>G NCBI36
NG_013375.1:g.85171C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.998+57C>G MANE Select ENSP00000297293.5:n.998+57C>G
ENST00000297293.5:c.998+57C>G ENSP00000297293.5:n.998+57C>G
NM_014916.3:c.998+57C>G NP_055731.2:n.998+57C>G
XM_011515981.1:c.992+57C>G XP_011514283.1:n.992+57C>G
XM_011515981.3:c.992+57C>G XP_011514283.1:n.992+57C>G
NM_014916.4:c.998+57C>G MANE Select NP_055731.2:n.998+57C>G
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