Canonical Allele Identifier: CA350097154
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129555A>T , CM000664.2:g.208129555A>T GRCh38
NC_000002.11:g.208994279A>T , CM000664.1:g.208994279A>T GRCh37
NC_000002.10:g.208702524A>T NCBI36
NG_008038.1:g.5276T>A
NG_008039.1:g.35T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.138T>A MANE Select ENSP00000282141.3:p.Tyr46Ter
ENST00000282141.3:c.138T>A ENSP00000282141.3:p.Tyr46Ter
NM_020989.3:c.138T>A NP_066269.1:p.Tyr46Ter
NR_038437.1:n.98-7501A>T
XM_011510661.1:c.138T>A XP_011508963.1:p.Tyr46Ter
XM_011510662.1:c.138T>A XP_011508964.1:p.Tyr46Ter
XM_011510663.1:c.9T>A XP_011508965.1:p.Tyr3Ter
NM_020989.4:c.138T>A MANE Select NP_066269.1:p.Tyr46Ter