Canonical Allele Identifier: CA350097681
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129682A>T , CM000664.2:g.208129682A>T GRCh38
NC_000002.11:g.208994406A>T , CM000664.1:g.208994406A>T GRCh37
NC_000002.10:g.208702651A>T NCBI36
NG_008038.1:g.5149T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.11T>A MANE Select ENSP00000282141.3:p.Ile4Asn
ENST00000282141.3:c.11T>A ENSP00000282141.3:p.Ile4Asn
NM_020989.3:c.11T>A NP_066269.1:p.Ile4Asn
NR_038437.1:n.98-7374A>T
XM_011510661.1:c.11T>A XP_011508963.1:p.Ile4Asn
XM_011510662.1:c.11T>A XP_011508964.1:p.Ile4Asn
XM_011510663.1:c.-119T>A XP_011508965.1:n.-119T>A
NM_020989.4:c.11T>A MANE Select NP_066269.1:p.Ile4Asn