Canonical Allele Identifier: CA1118964621

Gene: PRNCR1

Linked Data

• dbSNP Id: rs1813774639
• gnomAD v3: 8-127092012-C-T
• gnomAD v4: 8-127092012-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127092012C>T , CM000670.2:g.127092012C>T	GRCh38
NC_000008.10:g.128104257C>T , CM000670.1:g.128104257C>T	GRCh37
NC_000008.9:g.128173439C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.12139C>T