Canonical Allele Identifier: CA1323931477
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129649C= , CM000664.2:g.208129649C= GRCh38
NC_000002.11:g.208994373C= , CM000664.1:g.208994373C= GRCh37
NC_000002.10:g.208702618C= NCBI36
NG_008038.1:g.5182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.44G= MANE Select ENSP00000282141.3:p.Arg15=
ENST00000282141.3:c.44G= ENSP00000282141.3:p.Arg15=
NM_020989.3:c.44G= NP_066269.1:p.Arg15=
NR_038437.1:n.98-7407C=
XM_011510661.1:c.44G= XP_011508963.1:p.Arg15=
XM_011510662.1:c.44G= XP_011508964.1:p.Arg15=
XM_011510663.1:c.-86G= XP_011508965.1:n.-86G=
NM_020989.4:c.44G= MANE Select NP_066269.1:p.Arg15=