Canonical Allele Identifier: CA350092556
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.203A>G MANE Select ENSP00000264376.4:p.Gln68Arg
ENST00000264376.4:c.203A>G ENSP00000264376.4:p.Gln68Arg
NM_006891.3:c.203A>G NP_008822.2:p.Gln68Arg
NR_038437.1:n.97+4936T>C
NM_006891.4:c.203A>G MANE Select NP_008822.2:p.Gln68Arg