Canonical Allele Identifier: CA1323931530
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129749T= , CM000664.2:g.208129749T= GRCh38
NC_000002.11:g.208994473T= , CM000664.1:g.208994473T= GRCh37
NC_000002.10:g.208702718T= NCBI36
NG_008038.1:g.5082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.9+35A= MANE Select ENSP00000282141.3:n.9+35A=
ENST00000282141.3:c.9+35A= ENSP00000282141.3:n.9+35A=
NM_020989.3:c.9+35A= NP_066269.1:n.9+35A=
NR_038437.1:n.98-7307T=
XM_011510661.1:c.9+35A= XP_011508963.1:n.9+35A=
XM_011510662.1:c.9+35A= XP_011508964.1:n.9+35A=
XM_011510663.1:c.-120-66A= XP_011508965.1:n.-120-66A=
NM_020989.4:c.9+35A= MANE Select NP_066269.1:n.9+35A=