Canonical Allele Identifier: CA1323931445
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129584G= , CM000664.2:g.208129584G= GRCh38
NC_000002.11:g.208994308G= , CM000664.1:g.208994308G= GRCh37
NC_000002.10:g.208702553G= NCBI36
NG_008038.1:g.5247C=
NG_008039.1:g.6C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.109C= MANE Select ENSP00000282141.3:p.Arg37=
ENST00000282141.3:c.109C= ENSP00000282141.3:p.Arg37=
NM_020989.3:c.109C= NP_066269.1:p.Arg37=
NR_038437.1:n.98-7472G=
XM_011510661.1:c.109C= XP_011508963.1:p.Arg37=
XM_011510662.1:c.109C= XP_011508964.1:p.Arg37=
XM_011510663.1:c.-21C= XP_011508965.1:n.-21C=
NM_020989.4:c.109C= MANE Select NP_066269.1:p.Arg37=