Canonical Allele Identifier: CA2662867525

Gene: CRYGD

Linked Data

• gnomAD v4: 2-208124040-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124040T>C , CM000664.2:g.208124040T>C	GRCh38
NC_000002.11:g.208988764T>C , CM000664.1:g.208988764T>C	GRCh37
NC_000002.10:g.208697009T>C	NCBI36
NG_008039.1:g.5550A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+72A>G MANE Select	ENSP00000264376.4:n.252+72A>G
ENST00000264376.4:c.252+72A>G	ENSP00000264376.4:n.252+72A>G
NM_006891.3:c.252+72A>G	NP_008822.2:n.252+72A>G
NR_038437.1:n.97+4815T>C
NM_006891.4:c.252+72A>G MANE Select	NP_008822.2:n.252+72A>G