Canonical Allele Identifier: CA1323928966
Gene: CRYGD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124318G= , CM000664.2:g.208124318G= GRCh38
NC_000002.11:g.208989042G= , CM000664.1:g.208989042G= GRCh37
NC_000002.10:g.208697287G= NCBI36
NG_008039.1:g.5272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.46C= MANE Select ENSP00000264376.4:p.His16=
ENST00000264376.4:c.46C= ENSP00000264376.4:p.His16=
NM_006891.3:c.46C= NP_008822.2:p.His16=
NR_038437.1:n.97+5093G=
NM_006891.4:c.46C= MANE Select NP_008822.2:p.His16=
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