Canonical Allele Identifier: CA6722473
Gene: KRT19P2 HGNC NCBI
MIR492 HGNC NCBI
COSMIC:
COSN164323 (not active)
COSN15315417 (not active)
COSN19700415 (not active)
COSN20087948 (not active)
MyVariant.info:
GRCh38 chr12:g.94834510G>C
GRCh37 chr12:g.95228286G>C
gnomAD v2:
12:95228286 G / C
gnomAD v3:
12:94834510 G / C
gnomAD v4:
chr12-94834510-G-C
Joint Max Group AF 0.23482549 (EAS)
Genomes Max Group AF 0.23546272 (EAS)
Exomes Max Group AF 0.2318194 (EAS)
dbSNP:
2289030
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.94834510G>C , CM000674.2:g.94834510G>C GRCh38
NC_000012.11:g.95228286G>C , CM000674.1:g.95228286G>C GRCh37
NC_000012.10:g.93752417G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405395.2:n.57G>C (KRT19P2)
ENST00000557173.1:n.364G>C (KRT19P2)
NR_030171.1:n.113G>C (MIR492)
NR_036685.1:n.57G>C (KRT19P2)
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