Canonical Allele Identifier: CA1323931449
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129593T= , CM000664.2:g.208129593T= GRCh38
NC_000002.11:g.208994317T= , CM000664.1:g.208994317T= GRCh37
NC_000002.10:g.208702562T= NCBI36
NG_008038.1:g.5238A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.100A= MANE Select ENSP00000282141.3:p.Asn34=
ENST00000282141.3:c.100A= ENSP00000282141.3:p.Asn34=
NM_020989.3:c.100A= NP_066269.1:p.Asn34=
NR_038437.1:n.98-7463T=
XM_011510661.1:c.100A= XP_011508963.1:p.Asn34=
XM_011510662.1:c.100A= XP_011508964.1:p.Asn34=
XM_011510663.1:c.-30A= XP_011508965.1:n.-30A=
NM_020989.4:c.100A= MANE Select NP_066269.1:p.Asn34=