Canonical Allele Identifier: CA2640009322

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76540026-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540026C>T , CM000679.2:g.76540026C>T	GRCh38
NC_000017.10:g.74536108C>T , CM000679.1:g.74536108C>T	GRCh37
NC_000017.9:g.72047703C>T	NCBI36
NG_016702.1:g.17441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-479C>T (PRCD)
ENST00000465808.7:n.93-479C>T (PRCD)
ENST00000589145.1:c.-52-8335G>A (CYGB)	ENSP00000468559.1:n.-52-8335G>A
ENST00000590555.5:n.445-479C>T (PRCD)
ENST00000592432.5:n.249-479C>T (PRCD)
NR_033357.1:n.249-479C>T (PRCD)
XM_011524272.1:c.-52-8335G>A (CYGB)	XP_011522574.1:n.-52-8335G>A
XM_011525184.1:c.14-6C>T (PRCD)	XP_011523486.1:n.14-6C>T
XM_017024116.1:c.-52-8335G>A (CYGB)	XP_016879605.1:n.-52-8335G>A
XM_017025013.1:c.-116C>T (PRCD)	XP_016880502.1:n.-116C>T
XM_017025014.1:c.-116C>T (PRCD)	XP_016880503.1:n.-116C>T
XM_017025015.1:c.-116C>T (PRCD)	XP_016880504.1:n.-116C>T
NR_033357.2:n.249-479C>T (PRCD)