Canonical Allele Identifier: CA1323931493
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129681G= , CM000664.2:g.208129681G= GRCh38
NC_000002.11:g.208994405G= , CM000664.1:g.208994405G= GRCh37
NC_000002.10:g.208702650G= NCBI36
NG_008038.1:g.5150C=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.12C= MANE Select ENSP00000282141.3:p.Ile4=
ENST00000282141.3:c.12C= ENSP00000282141.3:p.Ile4=
NM_020989.3:c.12C= NP_066269.1:p.Ile4=
NR_038437.1:n.98-7375G=
XM_011510661.1:c.12C= XP_011508963.1:p.Ile4=
XM_011510662.1:c.12C= XP_011508964.1:p.Ile4=
XM_011510663.1:c.-118C= XP_011508965.1:n.-118C=
NM_020989.4:c.12C= MANE Select NP_066269.1:p.Ile4=