Canonical Allele Identifier: CA350092469
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208124120del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124120del , CM000664.2:g.208124120del GRCh38
NC_000002.11:g.208988844del , CM000664.1:g.208988844del GRCh37
NC_000002.10:g.208697089del NCBI36
NG_008039.1:g.5470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.244del MANE Select ENSP00000264376.4:p.Ile82SerfsTer21
ENST00000264376.4:c.244del ENSP00000264376.4:p.Ile82SerfsTer21
NM_006891.3:c.244del NP_008822.2:p.Ile82SerfsTer21
NR_038437.1:n.97+4895del
NM_006891.4:c.244del MANE Select NP_008822.2:p.Ile82SerfsTer21
Search 100 bp 5'
Search 100 bp 3'