Canonical Allele Identifier: CA350097692
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129685T>G , CM000664.2:g.208129685T>G GRCh38
NC_000002.11:g.208994409T>G , CM000664.1:g.208994409T>G GRCh37
NC_000002.10:g.208702654T>G NCBI36
NG_008038.1:g.5146A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-2A>C MANE Select ENSP00000282141.3:n.10-2A>C
ENST00000282141.3:c.10-2A>C ENSP00000282141.3:n.10-2A>C
NM_020989.3:c.10-2A>C NP_066269.1:n.10-2A>C
NR_038437.1:n.98-7371T>G
XM_011510661.1:c.10-2A>C XP_011508963.1:n.10-2A>C
XM_011510662.1:c.10-2A>C XP_011508964.1:n.10-2A>C
XM_011510663.1:c.-120-2A>C XP_011508965.1:n.-120-2A>C
NM_020989.4:c.10-2A>C MANE Select NP_066269.1:n.10-2A>C