Canonical Allele Identifier: CA401180854

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs1201369416
• gnomAD v2: 17-74536252-C-A
• gnomAD v4: 17-76540170-C-A
• MyVariant Identifiers: chr17:g.74536252C>A (hg19) ; chr17:g.76540170C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540170C>A , CM000679.2:g.76540170C>A	GRCh38
NC_000017.10:g.74536252C>A , CM000679.1:g.74536252C>A	GRCh37
NC_000017.9:g.72047847C>A	NCBI36
NG_016702.1:g.17585C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.29C>A (PRCD) MANE Select	ENSP00000467661.1:p.Thr10Asn
ENST00000397633.7:n.46-335C>A (PRCD)
ENST00000465808.7:n.93-335C>A (PRCD)
ENST00000586148.1:c.29C>A (PRCD)	ENSP00000465932.1:p.Thr10Asn
ENST00000589145.1:c.-52-8479G>T (CYGB)	ENSP00000468559.1:n.-52-8479G>T
ENST00000590555.5:n.445-335C>A (PRCD)
ENST00000592014.5:c.29C>A (PRCD)	ENSP00000467661.1:p.Thr10Asn
ENST00000592432.5:n.249-335C>A (PRCD)
NM_001077620.2:c.29C>A (PRCD)	NP_001071088.1:p.Thr10Asn
NR_033357.1:n.249-335C>A (PRCD)
XM_011524272.1:c.-52-8479G>T (CYGB)	XP_011522574.1:n.-52-8479G>T
XM_011525184.1:c.152C>A (PRCD)	XP_011523486.1:p.Thr51Asn
XM_017024116.1:c.-52-8479G>T (CYGB)	XP_016879605.1:n.-52-8479G>T
XM_017025013.1:c.29C>A (PRCD)	XP_016880502.1:p.Thr10Asn
XM_017025014.1:c.29C>A (PRCD)	XP_016880503.1:p.Thr10Asn
XM_017025015.1:c.29C>A (PRCD)	XP_016880504.1:p.Thr10Asn
NM_001077620.3:c.29C>A (PRCD) MANE Select	NP_001071088.1:p.Thr10Asn
NR_033357.2:n.249-335C>A (PRCD)