Canonical Allele Identifier: CA350092573
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124168G>C , CM000664.2:g.208124168G>C GRCh38
NC_000002.11:g.208988892G>C , CM000664.1:g.208988892G>C GRCh37
NC_000002.10:g.208697137G>C NCBI36
NG_008039.1:g.5422C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.196C>G MANE Select ENSP00000264376.4:p.His66Asp
ENST00000264376.4:c.196C>G ENSP00000264376.4:p.His66Asp
NM_006891.3:c.196C>G NP_008822.2:p.His66Asp
NR_038437.1:n.97+4943G>C
NM_006891.4:c.196C>G MANE Select NP_008822.2:p.His66Asp