Canonical Allele Identifier: CA1323931496
Gene: CRYGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129688A= , CM000664.2:g.208129688A= GRCh38
NC_000002.11:g.208994412A= , CM000664.1:g.208994412A= GRCh37
NC_000002.10:g.208702657A= NCBI36
NG_008038.1:g.5143T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.10-5T= MANE Select ENSP00000282141.3:n.10-5T=
ENST00000282141.3:c.10-5T= ENSP00000282141.3:n.10-5T=
NM_020989.3:c.10-5T= NP_066269.1:n.10-5T=
NR_038437.1:n.98-7368A=
XM_011510661.1:c.10-5T= XP_011508963.1:n.10-5T=
XM_011510662.1:c.10-5T= XP_011508964.1:n.10-5T=
XM_011510663.1:c.-120-5T= XP_011508965.1:n.-120-5T=
NM_020989.4:c.10-5T= MANE Select NP_066269.1:n.10-5T=