Canonical Allele Identifier: CA2077718
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs755012034
ExAC: 2:208988920 G / GTAC
gnomAD v2: 2-208988920-G-GTAC
gnomAD v3: 2-208124196-G-GTAC
gnomAD v4: 2-208124196-G-GTAC
MyVariant Identifiers: chr2:g.208988920_208988921insTAC (hg19) chr2:g.208124196_208124197insTAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124198_208124200dup , CM000664.2:g.208124198_208124200dup GRCh38
NC_000002.11:g.208988922_208988924dup , CM000664.1:g.208988922_208988924dup GRCh37
NC_000002.10:g.208697167_208697169dup NCBI36
NG_008039.1:g.5391_5393dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.165_167dup MANE Select ENSP00000264376.4:p.Tyr56Ter
ENST00000264376.4:c.165_167dup ENSP00000264376.4:p.Tyr56Ter
NM_006891.3:c.165_167dup NP_008822.2:p.Tyr56Ter
NR_038437.1:n.97+4973_97+4975dup
NM_006891.4:c.165_167dup MANE Select NP_008822.2:p.Tyr56Ter
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