Canonical Allele Identifier: CA350093119
Gene: CRYGD HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208989057C>G (hg19) chr2:g.208124333C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124333C>G , CM000664.2:g.208124333C>G GRCh38
NC_000002.11:g.208989057C>G , CM000664.1:g.208989057C>G GRCh37
NC_000002.10:g.208697302C>G NCBI36
NG_008039.1:g.5257G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.31G>C MANE Select ENSP00000264376.4:p.Gly11Arg
ENST00000264376.4:c.31G>C ENSP00000264376.4:p.Gly11Arg
NM_006891.3:c.31G>C NP_008822.2:p.Gly11Arg
NR_038437.1:n.97+5108C>G
NM_006891.4:c.31G>C MANE Select NP_008822.2:p.Gly11Arg
Search 100 bp 5'
Search 100 bp 3'