Canonical Allele Identifier: CA1323928858
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs1243350443
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124118del , CM000664.2:g.208124118del GRCh38
NC_000002.11:g.208988842del , CM000664.1:g.208988842del GRCh37
NC_000002.10:g.208697087del NCBI36
NG_008039.1:g.5476del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.250del MANE Select ENSP00000264376.4:p.His84ThrfsTer19
ENST00000264376.4:c.250del ENSP00000264376.4:p.His84ThrfsTer19
NM_006891.3:c.250del NP_008822.2:p.His84ThrfsTer19
NR_038437.1:n.97+4893del
NM_006891.4:c.250del MANE Select NP_008822.2:p.His84ThrfsTer19
Search 100 bp 5'
Search 100 bp 3'