Canonical Allele Identifier: CA12598186
Gene: LINC-PINT HGNC NCBI
COSMIC:
COSN17133684 (not active)
COSN17134530 (not active)
COSN17136331 (not active)
COSN17138225 (not active)
COSN17140015 (not active)
COSN17140866 (not active)
COSN17141868 (not active)
COSN17143140 (not active)
COSN17145780 (not active)
COSN17146686 (not active)
COSN17149355 (not active)
COSN17151207 (not active)
MyVariant.info:
GRCh38 chr7:g.130969092C>A
GRCh37 chr7:g.130653851C>A
gnomAD v2:
7:130653851 C / A
gnomAD v3:
7:130969092 C / A
gnomAD v4:
chr7-130969092-C-A
Joint Max Group AF 0.70389299 (AFR)
Genomes Max Group AF 0.70389299 (AFR)
dbSNP:
2048672
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.130969092C>A , CM000669.2:g.130969092C>A GRCh38
NC_000007.13:g.130653851C>A , CM000669.1:g.130653851C>A GRCh37
NC_000007.12:g.130304391C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015431.2:n.1452+14961G>T
NR_024153.2:n.418+14961G>T
NR_109850.1:n.1576+14961G>T
NR_109851.1:n.1453-1575G>T
NR_109852.1:n.1453-9122G>T
NR_109853.1:n.1452+14961G>T
NR_109854.1:n.1452+14961G>T
NR_109855.1:n.1321+14961G>T
NR_170175.1:n.1606+9416G>T
NR_170176.1:n.1482+9416G>T
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