Canonical Allele Identifier: CA481503344

Gene: KRT19P2 MIR492

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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