Canonical Allele Identifier: CA2055971542
Community Standard Title: NC_000012.12:g.94834510G=
Gene: KRT19P2 HGNC NCBI
MIR492 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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