Canonical Allele Identifier: CA1323928879
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124158C= , CM000664.2:g.208124158C= GRCh38
NC_000002.11:g.208988882C= , CM000664.1:g.208988882C= GRCh37
NC_000002.10:g.208697127C= NCBI36
NG_008039.1:g.5432G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.206G= MANE Select ENSP00000264376.4:p.Trp69=
ENST00000264376.4:c.206G= ENSP00000264376.4:p.Trp69=
NM_006891.3:c.206G= NP_008822.2:p.Trp69=
NR_038437.1:n.97+4933C=
NM_006891.4:c.206G= MANE Select NP_008822.2:p.Trp69=