Canonical Allele Identifier: CA1323928783
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208123993T= , CM000664.2:g.208123993T= GRCh38
NC_000002.11:g.208988717T= , CM000664.1:g.208988717T= GRCh37
NC_000002.10:g.208696962T= NCBI36
NG_008039.1:g.5597A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+119A= MANE Select ENSP00000264376.4:n.252+119A=
ENST00000264376.4:c.252+119A= ENSP00000264376.4:n.252+119A=
NM_006891.3:c.252+119A= NP_008822.2:n.252+119A=
NR_038437.1:n.97+4768T=
NM_006891.4:c.252+119A= MANE Select NP_008822.2:n.252+119A=
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