Canonical Allele Identifier: CA1323931451
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129595C= , CM000664.2:g.208129595C= GRCh38
NC_000002.11:g.208994319C= , CM000664.1:g.208994319C= GRCh37
NC_000002.10:g.208702564C= NCBI36
NG_008038.1:g.5236G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.98G= MANE Select ENSP00000282141.3:p.Cys33=
ENST00000282141.3:c.98G= ENSP00000282141.3:p.Cys33=
NM_020989.3:c.98G= NP_066269.1:p.Cys33=
NR_038437.1:n.98-7461C=
XM_011510661.1:c.98G= XP_011508963.1:p.Cys33=
XM_011510662.1:c.98G= XP_011508964.1:p.Cys33=
XM_011510663.1:c.-32G= XP_011508965.1:n.-32G=
NM_020989.4:c.98G= MANE Select NP_066269.1:p.Cys33=