Canonical Allele Identifier: CA1323928923
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124232C= , CM000664.2:g.208124232C= GRCh38
NC_000002.11:g.208988956C= , CM000664.1:g.208988956C= GRCh37
NC_000002.10:g.208697201C= NCBI36
NG_008039.1:g.5358G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.132G= MANE Select ENSP00000264376.4:p.Met44=
ENST00000264376.4:c.132G= ENSP00000264376.4:p.Met44=
NM_006891.3:c.132G= NP_008822.2:p.Met44=
NR_038437.1:n.97+5007C=
NM_006891.4:c.132G= MANE Select NP_008822.2:p.Met44=
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