Canonical Allele Identifier: CA1323928903
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124193G= , CM000664.2:g.208124193G= GRCh38
NC_000002.11:g.208988917G= , CM000664.1:g.208988917G= GRCh37
NC_000002.10:g.208697162G= NCBI36
NG_008039.1:g.5397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.171C= MANE Select ENSP00000264376.4:p.Phe57=
ENST00000264376.4:c.171C= ENSP00000264376.4:p.Phe57=
NM_006891.3:c.171C= NP_008822.2:p.Phe57=
NR_038437.1:n.97+4968G=
NM_006891.4:c.171C= MANE Select NP_008822.2:p.Phe57=