Canonical Allele Identifier: CA2688538000

Gene: PRNCR1

Linked Data

• dbSNP Id: rs2130317612
• gnomAD v4: 8-127092091-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092091A>G , CM000670.2:g.127092091A>G	GRCh38
NC_000008.10:g.128104336A>G , CM000670.1:g.128104336A>G	GRCh37
NC_000008.9:g.128173518A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12218A>G