Canonical Allele Identifier: CA12798056

Gene: PRNCR1

Linked Data

• dbSNP Id: rs7001895
• gnomAD v2: 8-128103679-G-C
• gnomAD v3: 8-127091434-G-C
• gnomAD v4: 8-127091434-G-C
• MyVariant Identifiers: chr8:g.128103679G>C (hg19) ; chr8:g.127091434G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127091434G>C , CM000670.2:g.127091434G>C	GRCh38
NC_000008.10:g.128103679G>C , CM000670.1:g.128103679G>C	GRCh37
NC_000008.9:g.128172861G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109833.1:n.11561G>C