Canonical Allele Identifier: CA1323928779

Gene: CRYGD

Linked Data

• dbSNP Id: rs971006188
• gnomAD v4: 2-208123988-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208123988A>C , CM000664.2:g.208123988A>C	GRCh38
NC_000002.11:g.208988712A>C , CM000664.1:g.208988712A>C	GRCh37
NC_000002.10:g.208696957A>C	NCBI36
NG_008039.1:g.5602T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+124T>G MANE Select	ENSP00000264376.4:n.252+124T>G
ENST00000264376.4:c.252+124T>G	ENSP00000264376.4:n.252+124T>G
NM_006891.3:c.252+124T>G	NP_008822.2:n.252+124T>G
NR_038437.1:n.97+4763A>C
NM_006891.4:c.252+124T>G MANE Select	NP_008822.2:n.252+124T>G