Canonical Allele Identifier: CA2662867421

Gene: CRYGD

Linked Data

• gnomAD v4: 2-208123994-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208123994C>T , CM000664.2:g.208123994C>T	GRCh38
NC_000002.11:g.208988718C>T , CM000664.1:g.208988718C>T	GRCh37
NC_000002.10:g.208696963C>T	NCBI36
NG_008039.1:g.5596G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+118G>A MANE Select	ENSP00000264376.4:n.252+118G>A
ENST00000264376.4:c.252+118G>A	ENSP00000264376.4:n.252+118G>A
NM_006891.3:c.252+118G>A	NP_008822.2:n.252+118G>A
NR_038437.1:n.97+4769C>T
NM_006891.4:c.252+118G>A MANE Select	NP_008822.2:n.252+118G>A