Canonical Allele Identifier: CA350097691
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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