Canonical Allele Identifier: CA1323928798
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124013G= , CM000664.2:g.208124013G= GRCh38
NC_000002.11:g.208988737G= , CM000664.1:g.208988737G= GRCh37
NC_000002.10:g.208696982G= NCBI36
NG_008039.1:g.5577C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+99C= MANE Select ENSP00000264376.4:n.252+99C=
ENST00000264376.4:c.252+99C= ENSP00000264376.4:n.252+99C=
NM_006891.3:c.252+99C= NP_008822.2:n.252+99C=
NR_038437.1:n.97+4788G=
NM_006891.4:c.252+99C= MANE Select NP_008822.2:n.252+99C=
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