Canonical Allele Identifier: CA1323931423
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129549A= , CM000664.2:g.208129549A= GRCh38
NC_000002.11:g.208994273A= , CM000664.1:g.208994273A= GRCh37
NC_000002.10:g.208702518A= NCBI36
NG_008038.1:g.5282T=
NG_008039.1:g.41T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.144T= MANE Select ENSP00000282141.3:p.Arg48=
ENST00000282141.3:c.144T= ENSP00000282141.3:p.Arg48=
NM_020989.3:c.144T= NP_066269.1:p.Arg48=
NR_038437.1:n.98-7507A=
XM_011510661.1:c.144T= XP_011508963.1:p.Arg48=
XM_011510662.1:c.144T= XP_011508964.1:p.Arg48=
XM_011510663.1:c.15T= XP_011508965.1:p.Arg5=
NM_020989.4:c.144T= MANE Select NP_066269.1:p.Arg48=