Canonical Allele Identifier: CA401182283

Gene: PRCD CYGB

Linked Data

• dbSNP Id: rs2074978469
• MyVariant Identifiers: chr17:g.74536603G>C (hg19) ; chr17:g.76540521G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76540521G>C , CM000679.2:g.76540521G>C	GRCh38
NC_000017.10:g.74536603G>C , CM000679.1:g.74536603G>C	GRCh37
NC_000017.9:g.72048198G>C	NCBI36
NG_016702.1:g.17936G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592014.6:c.91G>C (PRCD) MANE Select	ENSP00000467661.1:p.Asp31His
ENST00000397630.7:n.51G>C (PRCD)
ENST00000397633.7:n.62G>C (PRCD)
ENST00000465808.7:n.109G>C (PRCD)
ENST00000586148.1:c.91G>C (PRCD)	ENSP00000465932.1:p.Asp31His
ENST00000589145.1:c.-52-8830C>G (CYGB)	ENSP00000468559.1:n.-52-8830C>G
ENST00000590555.5:n.461G>C (PRCD)
ENST00000592014.5:c.91G>C (PRCD)	ENSP00000467661.1:p.Asp31His
ENST00000592432.5:n.265G>C (PRCD)
NM_001077620.2:c.91G>C (PRCD)	NP_001071088.1:p.Asp31His
NR_033357.1:n.265G>C (PRCD)
XM_011524272.1:c.-52-8830C>G (CYGB)	XP_011522574.1:n.-52-8830C>G
XM_011525184.1:c.214G>C (PRCD)	XP_011523486.1:p.Asp72His
XM_017024116.1:c.-52-8830C>G (CYGB)	XP_016879605.1:n.-52-8830C>G
XM_017025013.1:c.91G>C (PRCD)	XP_016880502.1:p.Asp31His
XM_017025014.1:c.91G>C (PRCD)	XP_016880503.1:p.Asp31His
XM_017025015.1:c.91G>C (PRCD)	XP_016880504.1:p.Asp31His
NM_001077620.3:c.91G>C (PRCD) MANE Select	NP_001071088.1:p.Asp31His
NR_033357.2:n.265G>C (PRCD)