Canonical Allele Identifier: CA350097416
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129608A>G , CM000664.2:g.208129608A>G GRCh38
NC_000002.11:g.208994332A>G , CM000664.1:g.208994332A>G GRCh37
NC_000002.10:g.208702577A>G NCBI36
NG_008038.1:g.5223T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.85T>C MANE Select ENSP00000282141.3:p.Tyr29His
ENST00000282141.3:c.85T>C ENSP00000282141.3:p.Tyr29His
NM_020989.3:c.85T>C NP_066269.1:p.Tyr29His
NR_038437.1:n.98-7448A>G
XM_011510661.1:c.85T>C XP_011508963.1:p.Tyr29His
XM_011510662.1:c.85T>C XP_011508964.1:p.Tyr29His
XM_011510663.1:c.-45T>C XP_011508965.1:n.-45T>C
NM_020989.4:c.85T>C MANE Select NP_066269.1:p.Tyr29His