Canonical Allele Identifier: CA1323928882
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124161T= , CM000664.2:g.208124161T= GRCh38
NC_000002.11:g.208988885T= , CM000664.1:g.208988885T= GRCh37
NC_000002.10:g.208697130T= NCBI36
NG_008039.1:g.5429A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.203A= MANE Select ENSP00000264376.4:p.Gln68=
ENST00000264376.4:c.203A= ENSP00000264376.4:p.Gln68=
NM_006891.3:c.203A= NP_008822.2:p.Gln68=
NR_038437.1:n.97+4936T=
NM_006891.4:c.203A= MANE Select NP_008822.2:p.Gln68=