Canonical Allele Identifier: CA1323931503
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129703C= , CM000664.2:g.208129703C= GRCh38
NC_000002.11:g.208994427C= , CM000664.1:g.208994427C= GRCh37
NC_000002.10:g.208702672C= NCBI36
NG_008038.1:g.5128G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-20G= MANE Select ENSP00000282141.3:n.10-20G=
ENST00000282141.3:c.10-20G= ENSP00000282141.3:n.10-20G=
NM_020989.3:c.10-20G= NP_066269.1:n.10-20G=
NR_038437.1:n.98-7353C=
XM_011510661.1:c.10-20G= XP_011508963.1:n.10-20G=
XM_011510662.1:c.10-20G= XP_011508964.1:n.10-20G=
XM_011510663.1:c.-120-20G= XP_011508965.1:n.-120-20G=
NM_020989.4:c.10-20G= MANE Select NP_066269.1:n.10-20G=