Canonical Allele Identifier: CA1323928789

Gene: CRYGD

Linked Data

• dbSNP Id: rs1694923347
• gnomAD v4: 2-208124007-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124007C>T , CM000664.2:g.208124007C>T	GRCh38
NC_000002.11:g.208988731C>T , CM000664.1:g.208988731C>T	GRCh37
NC_000002.10:g.208696976C>T	NCBI36
NG_008039.1:g.5583G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+105G>A MANE Select	ENSP00000264376.4:n.252+105G>A
ENST00000264376.4:c.252+105G>A	ENSP00000264376.4:n.252+105G>A
NM_006891.3:c.252+105G>A	NP_008822.2:n.252+105G>A
NR_038437.1:n.97+4782C>T
NM_006891.4:c.252+105G>A MANE Select	NP_008822.2:n.252+105G>A