Canonical Allele Identifier: CA2577225866
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124019G>T , CM000664.2:g.208124019G>T GRCh38
NC_000002.11:g.208988743G>T , CM000664.1:g.208988743G>T GRCh37
NC_000002.10:g.208696988G>T NCBI36
NG_008039.1:g.5571C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+93C>A MANE Select ENSP00000264376.4:n.252+93C>A
ENST00000264376.4:c.252+93C>A ENSP00000264376.4:n.252+93C>A
NM_006891.3:c.252+93C>A NP_008822.2:n.252+93C>A
NR_038437.1:n.97+4794G>T
NM_006891.4:c.252+93C>A MANE Select NP_008822.2:n.252+93C>A