Canonical Allele Identifier: CA2683855049
Gene: LMTK2 HGNC NCBI

Linked Data

gnomAD v4: 7-98186839-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186839A>T , CM000669.2:g.98186839A>T GRCh38
NC_000007.13:g.97816151A>T , CM000669.1:g.97816151A>T GRCh37
NC_000007.12:g.97654087A>T NCBI36
NG_013375.1:g.84955A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-38A>T MANE Select ENSP00000297293.5:n.877-38A>T
ENST00000297293.5:c.877-38A>T ENSP00000297293.5:n.877-38A>T
NM_014916.3:c.877-38A>T NP_055731.2:n.877-38A>T
XM_011515981.1:c.871-38A>T XP_011514283.1:n.871-38A>T
XM_011515981.3:c.871-38A>T XP_011514283.1:n.871-38A>T
NM_014916.4:c.877-38A>T MANE Select NP_055731.2:n.877-38A>T