Canonical Allele Identifier: CA847146680

Gene: PRNCR1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091692T>A , CM000670.2:g.127091692T>A	GRCh38
NC_000008.10:g.128103937T>A , CM000670.1:g.128103937T>A	GRCh37
NC_000008.9:g.128173119T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11819T>A