Canonical Allele Identifier: CA350092681
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124220C>G , CM000664.2:g.208124220C>G GRCh38
NC_000002.11:g.208988944C>G , CM000664.1:g.208988944C>G GRCh37
NC_000002.10:g.208697189C>G NCBI36
NG_008039.1:g.5370G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.144G>C MANE Select ENSP00000264376.4:p.Gln48His
ENST00000264376.4:c.144G>C ENSP00000264376.4:p.Gln48His
NM_006891.3:c.144G>C NP_008822.2:p.Gln48His
NR_038437.1:n.97+4995C>G
NM_006891.4:c.144G>C MANE Select NP_008822.2:p.Gln48His