Canonical Allele Identifier: CA2077924
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs558534216

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129500C>T , CM000664.2:g.208129500C>T GRCh38
NC_000002.11:g.208994224C>T , CM000664.1:g.208994224C>T GRCh37
NC_000002.10:g.208702469C>T NCBI36
NG_008038.1:g.5331G>A
NG_008039.1:g.90G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.193G>A MANE Select ENSP00000282141.3:p.Asp65Asn
ENST00000282141.3:c.193G>A ENSP00000282141.3:p.Asp65Asn
NM_020989.3:c.193G>A NP_066269.1:p.Asp65Asn
NR_038437.1:n.98-7556C>T
XM_011510661.1:c.193G>A XP_011508963.1:p.Asp65Asn
XM_011510662.1:c.193G>A XP_011508964.1:p.Asp65Asn
XM_011510663.1:c.64G>A XP_011508965.1:p.Asp22Asn
NM_020989.4:c.193G>A MANE Select NP_066269.1:p.Asp65Asn