Canonical Allele Identifier: CA2683854996
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98186766-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186766C>A , CM000669.2:g.98186766C>A GRCh38
NC_000007.13:g.97816078C>A , CM000669.1:g.97816078C>A GRCh37
NC_000007.12:g.97654014C>A NCBI36
NG_013375.1:g.84882C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-111C>A MANE Select ENSP00000297293.5:n.877-111C>A
ENST00000297293.5:c.877-111C>A ENSP00000297293.5:n.877-111C>A
NM_014916.3:c.877-111C>A NP_055731.2:n.877-111C>A
XM_011515981.1:c.871-111C>A XP_011514283.1:n.871-111C>A
XM_011515981.3:c.871-111C>A XP_011514283.1:n.871-111C>A
NM_014916.4:c.877-111C>A MANE Select NP_055731.2:n.877-111C>A
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Search 100 bp 3'