Canonical Allele Identifier: CA350092670
Gene: CRYGD HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.149A>T MANE Select ENSP00000264376.4:p.Asn50Ile
ENST00000264376.4:c.149A>T ENSP00000264376.4:p.Asn50Ile
NM_006891.3:c.149A>T NP_008822.2:p.Asn50Ile
NR_038437.1:n.97+4990T>A
NM_006891.4:c.149A>T MANE Select NP_008822.2:p.Asn50Ile