Canonical Allele Identifier: CA2662867423

Gene: CRYGD

Linked Data

• gnomAD v4: 2-208123995-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208123995A>C , CM000664.2:g.208123995A>C	GRCh38
NC_000002.11:g.208988719A>C , CM000664.1:g.208988719A>C	GRCh37
NC_000002.10:g.208696964A>C	NCBI36
NG_008039.1:g.5595T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+117T>G MANE Select	ENSP00000264376.4:n.252+117T>G
ENST00000264376.4:c.252+117T>G	ENSP00000264376.4:n.252+117T>G
NM_006891.3:c.252+117T>G	NP_008822.2:n.252+117T>G
NR_038437.1:n.97+4770A>C
NM_006891.4:c.252+117T>G MANE Select	NP_008822.2:n.252+117T>G