Canonical Allele Identifier: CA576377440

Gene: LMTK2

Linked Data

• dbSNP Id: rs1254043270
• gnomAD v2: 7-97816613-T-C
• gnomAD v3: 7-98187301-T-C
• gnomAD v4: 7-98187301-T-C
• MyVariant Identifiers: chr7:g.97816613T>C (hg19) ; chr7:g.98187301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.98187301T>C , CM000669.2:g.98187301T>C	GRCh38
NC_000007.13:g.97816613T>C , CM000669.1:g.97816613T>C	GRCh37
NC_000007.12:g.97654549T>C	NCBI36
NG_013375.1:g.85417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297293.6:c.998+303T>C MANE Select	ENSP00000297293.5:n.998+303T>C
ENST00000297293.5:c.998+303T>C	ENSP00000297293.5:n.998+303T>C
NM_014916.3:c.998+303T>C	NP_055731.2:n.998+303T>C
XM_011515981.1:c.992+303T>C	XP_011514283.1:n.992+303T>C
XM_011515981.3:c.992+303T>C	XP_011514283.1:n.992+303T>C
NM_014916.4:c.998+303T>C MANE Select	NP_055731.2:n.998+303T>C