Canonical Allele Identifier: CA1323928874
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124142G= , CM000664.2:g.208124142G= GRCh38
NC_000002.11:g.208988866G= , CM000664.1:g.208988866G= GRCh37
NC_000002.10:g.208697111G= NCBI36
NG_008039.1:g.5448C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.222C= MANE Select ENSP00000264376.4:p.Asp74=
ENST00000264376.4:c.222C= ENSP00000264376.4:p.Asp74=
NM_006891.3:c.222C= NP_008822.2:p.Asp74=
NR_038437.1:n.97+4917G=
NM_006891.4:c.222C= MANE Select NP_008822.2:p.Asp74=