Canonical Allele Identifier: CA64607688
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1027171227

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.203A>C MANE Select ENSP00000264376.4:p.Gln68Pro
ENST00000264376.4:c.203A>C ENSP00000264376.4:p.Gln68Pro
NM_006891.3:c.203A>C NP_008822.2:p.Gln68Pro
NR_038437.1:n.97+4936T>G
NM_006891.4:c.203A>C MANE Select NP_008822.2:p.Gln68Pro