Canonical Allele Identifier: CA2640009275

Gene: PRCD CYGB

Linked Data

• gnomAD v4: 17-76539997-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76539997T>A , CM000679.2:g.76539997T>A	GRCh38
NC_000017.10:g.74536079T>A , CM000679.1:g.74536079T>A	GRCh37
NC_000017.9:g.72047674T>A	NCBI36
NG_016702.1:g.17412T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397633.7:n.46-508T>A (PRCD)
ENST00000465808.7:n.93-508T>A (PRCD)
ENST00000589145.1:c.-52-8306A>T (CYGB)	ENSP00000468559.1:n.-52-8306A>T
ENST00000590555.5:n.445-508T>A (PRCD)
ENST00000592432.5:n.249-508T>A (PRCD)
NR_033357.1:n.249-508T>A (PRCD)
XM_011524272.1:c.-52-8306A>T (CYGB)	XP_011522574.1:n.-52-8306A>T
XM_011525184.1:c.14-35T>A (PRCD)	XP_011523486.1:n.14-35T>A
XM_017024116.1:c.-52-8306A>T (CYGB)	XP_016879605.1:n.-52-8306A>T
XM_017025013.1:c.-145T>A (PRCD)	XP_016880502.1:n.-145T>A
XM_017025014.1:c.-145T>A (PRCD)	XP_016880503.1:n.-145T>A
XM_017025015.1:c.-145T>A (PRCD)	XP_016880504.1:n.-145T>A
NR_033357.2:n.249-508T>A (PRCD)