Canonical Allele Identifier: CA1323931498
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129693A= , CM000664.2:g.208129693A= GRCh38
NC_000002.11:g.208994417A= , CM000664.1:g.208994417A= GRCh37
NC_000002.10:g.208702662A= NCBI36
NG_008038.1:g.5138T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-10T= MANE Select ENSP00000282141.3:n.10-10T=
ENST00000282141.3:c.10-10T= ENSP00000282141.3:n.10-10T=
NM_020989.3:c.10-10T= NP_066269.1:n.10-10T=
NR_038437.1:n.98-7363A=
XM_011510661.1:c.10-10T= XP_011508963.1:n.10-10T=
XM_011510662.1:c.10-10T= XP_011508964.1:n.10-10T=
XM_011510663.1:c.-120-10T= XP_011508965.1:n.-120-10T=
NM_020989.4:c.10-10T= MANE Select NP_066269.1:n.10-10T=