Canonical Allele Identifier: CA2077683

Gene: CRYGD

Linked Data

• dbSNP Id: rs770795833
• ExAC: 2:208988803 A / C
• gnomAD v2: 2-208988803-A-C
• gnomAD v4: 2-208124079-A-C
• MyVariant Identifiers: chr2:g.208988803A>C (hg19) ; chr2:g.208124079A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124079A>C , CM000664.2:g.208124079A>C	GRCh38
NC_000002.11:g.208988803A>C , CM000664.1:g.208988803A>C	GRCh37
NC_000002.10:g.208697048A>C	NCBI36
NG_008039.1:g.5511T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264376.5:c.252+33T>G MANE Select	ENSP00000264376.4:n.252+33T>G
ENST00000264376.4:c.252+33T>G	ENSP00000264376.4:n.252+33T>G
NM_006891.3:c.252+33T>G	NP_008822.2:n.252+33T>G
NR_038437.1:n.97+4854A>C
NM_006891.4:c.252+33T>G MANE Select	NP_008822.2:n.252+33T>G