Canonical Allele Identifier: CA1323931411
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129525G= , CM000664.2:g.208129525G= GRCh38
NC_000002.11:g.208994249G= , CM000664.1:g.208994249G= GRCh37
NC_000002.10:g.208702494G= NCBI36
NG_008038.1:g.5306C=
NG_008039.1:g.65C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.168C= MANE Select ENSP00000282141.3:p.Tyr56=
ENST00000282141.3:c.168C= ENSP00000282141.3:p.Tyr56=
NM_020989.3:c.168C= NP_066269.1:p.Tyr56=
NR_038437.1:n.98-7531G=
XM_011510661.1:c.168C= XP_011508963.1:p.Tyr56=
XM_011510662.1:c.168C= XP_011508964.1:p.Tyr56=
XM_011510663.1:c.39C= XP_011508965.1:p.Tyr13=
NM_020989.4:c.168C= MANE Select NP_066269.1:p.Tyr56=