Canonical Allele Identifier: CA350092479
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208988850G>T (hg19) chr2:g.208124126G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124126G>T , CM000664.2:g.208124126G>T GRCh38
NC_000002.11:g.208988850G>T , CM000664.1:g.208988850G>T GRCh37
NC_000002.10:g.208697095G>T NCBI36
NG_008039.1:g.5464C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.238C>A MANE Select ENSP00000264376.4:p.Arg80Ser
ENST00000264376.4:c.238C>A ENSP00000264376.4:p.Arg80Ser
NM_006891.3:c.238C>A NP_008822.2:p.Arg80Ser
NR_038437.1:n.97+4901G>T
NM_006891.4:c.238C>A MANE Select NP_008822.2:p.Arg80Ser
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