Canonical Allele Identifier: CA350092672
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1694932192

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124216T>C , CM000664.2:g.208124216T>C GRCh38
NC_000002.11:g.208988940T>C , CM000664.1:g.208988940T>C GRCh37
NC_000002.10:g.208697185T>C NCBI36
NG_008039.1:g.5374A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.148A>G MANE Select ENSP00000264376.4:p.Asn50Asp
ENST00000264376.4:c.148A>G ENSP00000264376.4:p.Asn50Asp
NM_006891.3:c.148A>G NP_008822.2:p.Asn50Asp
NR_038437.1:n.97+4991T>C
NM_006891.4:c.148A>G MANE Select NP_008822.2:p.Asn50Asp