Canonical Allele Identifier: CA1323928913
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124215T= , CM000664.2:g.208124215T= GRCh38
NC_000002.11:g.208988939T= , CM000664.1:g.208988939T= GRCh37
NC_000002.10:g.208697184T= NCBI36
NG_008039.1:g.5375A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.149A= MANE Select ENSP00000264376.4:p.Asn50=
ENST00000264376.4:c.149A= ENSP00000264376.4:p.Asn50=
NM_006891.3:c.149A= NP_008822.2:p.Asn50=
NR_038437.1:n.97+4990T=
NM_006891.4:c.149A= MANE Select NP_008822.2:p.Asn50=