Canonical Allele Identifier: CA1323928781
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208123992T= , CM000664.2:g.208123992T= GRCh38
NC_000002.11:g.208988716T= , CM000664.1:g.208988716T= GRCh37
NC_000002.10:g.208696961T= NCBI36
NG_008039.1:g.5598A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+120A= MANE Select ENSP00000264376.4:n.252+120A=
ENST00000264376.4:c.252+120A= ENSP00000264376.4:n.252+120A=
NM_006891.3:c.252+120A= NP_008822.2:n.252+120A=
NR_038437.1:n.97+4767T=
NM_006891.4:c.252+120A= MANE Select NP_008822.2:n.252+120A=
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