Canonical Allele Identifier: CA2662867541
Gene: CRYGD HGNC NCBI

Linked Data

gnomAD v4: 2-208124063-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124065del , CM000664.2:g.208124065del GRCh38
NC_000002.11:g.208988789del , CM000664.1:g.208988789del GRCh37
NC_000002.10:g.208697034del NCBI36
NG_008039.1:g.5526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+48del MANE Select ENSP00000264376.4:n.252+48del
ENST00000264376.4:c.252+48del ENSP00000264376.4:n.252+48del
NM_006891.3:c.252+48del NP_008822.2:n.252+48del
NR_038437.1:n.97+4840del
NM_006891.4:c.252+48del MANE Select NP_008822.2:n.252+48del
Search 100 bp 5'
Search 100 bp 3'