Canonical Allele Identifier: CA1323928787
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124006A= , CM000664.2:g.208124006A= GRCh38
NC_000002.11:g.208988730A= , CM000664.1:g.208988730A= GRCh37
NC_000002.10:g.208696975A= NCBI36
NG_008039.1:g.5584T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+106T= MANE Select ENSP00000264376.4:n.252+106T=
ENST00000264376.4:c.252+106T= ENSP00000264376.4:n.252+106T=
NM_006891.3:c.252+106T= NP_008822.2:n.252+106T=
NR_038437.1:n.97+4781A=
NM_006891.4:c.252+106T= MANE Select NP_008822.2:n.252+106T=
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