Canonical Allele Identifier: CA1323928973
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124328G= , CM000664.2:g.208124328G= GRCh38
NC_000002.11:g.208989052G= , CM000664.1:g.208989052G= GRCh37
NC_000002.10:g.208697297G= NCBI36
NG_008039.1:g.5262C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.36C= MANE Select ENSP00000264376.4:p.Phe12=
ENST00000264376.4:c.36C= ENSP00000264376.4:p.Phe12=
NM_006891.3:c.36C= NP_008822.2:p.Phe12=
NR_038437.1:n.97+5103G=
NM_006891.4:c.36C= MANE Select NP_008822.2:p.Phe12=
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