Canonical Allele Identifier: CA350097452
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129625C>T , CM000664.2:g.208129625C>T GRCh38
NC_000002.11:g.208994349C>T , CM000664.1:g.208994349C>T GRCh37
NC_000002.10:g.208702594C>T NCBI36
NG_008038.1:g.5206G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.68G>A MANE Select ENSP00000282141.3:p.Cys23Tyr
ENST00000282141.3:c.68G>A ENSP00000282141.3:p.Cys23Tyr
NM_020989.3:c.68G>A NP_066269.1:p.Cys23Tyr
NR_038437.1:n.98-7431C>T
XM_011510661.1:c.68G>A XP_011508963.1:p.Cys23Tyr
XM_011510662.1:c.68G>A XP_011508964.1:p.Cys23Tyr
XM_011510663.1:c.-62G>A XP_011508965.1:n.-62G>A
NM_020989.4:c.68G>A MANE Select NP_066269.1:p.Cys23Tyr