Canonical Allele Identifier: CA1323928778
Gene: CRYGD HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208123988A= , CM000664.2:g.208123988A= GRCh38
NC_000002.11:g.208988712A= , CM000664.1:g.208988712A= GRCh37
NC_000002.10:g.208696957A= NCBI36
NG_008039.1:g.5602T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+124T= MANE Select ENSP00000264376.4:n.252+124T=
ENST00000264376.4:c.252+124T= ENSP00000264376.4:n.252+124T=
NM_006891.3:c.252+124T= NP_008822.2:n.252+124T=
NR_038437.1:n.97+4763A=
NM_006891.4:c.252+124T= MANE Select NP_008822.2:n.252+124T=
Search 100 bp 5'
Search 100 bp 3'