Canonical Allele Identifier: CA350093094
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124329A>C , CM000664.2:g.208124329A>C GRCh38
NC_000002.11:g.208989053A>C , CM000664.1:g.208989053A>C GRCh37
NC_000002.10:g.208697298A>C NCBI36
NG_008039.1:g.5261T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.35T>G MANE Select ENSP00000264376.4:p.Phe12Cys
ENST00000264376.4:c.35T>G ENSP00000264376.4:p.Phe12Cys
NM_006891.3:c.35T>G NP_008822.2:p.Phe12Cys
NR_038437.1:n.97+5104A>C
NM_006891.4:c.35T>G MANE Select NP_008822.2:p.Phe12Cys