Canonical Allele Identifier: CA2688533290
Gene: PRNCR1 HGNC NCBI
PCAT2 HGNC NCBI

Linked Data

gnomAD v4: 8-127080067-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127080067A>C , CM000670.2:g.127080067A>C GRCh38
NC_000008.10:g.128092312A>C , CM000670.1:g.128092312A>C GRCh37
NC_000008.9:g.128161494A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109833.1:n.194A>C (PRNCR1)
NR_119373.1:n.102-934T>G (PCAT2)
Search 100 bp 5'
Search 100 bp 3'