Canonical Allele Identifier: CA350097356
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129591G>T , CM000664.2:g.208129591G>T GRCh38
NC_000002.11:g.208994315G>T , CM000664.1:g.208994315G>T GRCh37
NC_000002.10:g.208702560G>T NCBI36
NG_008038.1:g.5240C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.102C>A MANE Select ENSP00000282141.3:p.Asn34Lys
ENST00000282141.3:c.102C>A ENSP00000282141.3:p.Asn34Lys
NM_020989.3:c.102C>A NP_066269.1:p.Asn34Lys
NR_038437.1:n.98-7465G>T
XM_011510661.1:c.102C>A XP_011508963.1:p.Asn34Lys
XM_011510662.1:c.102C>A XP_011508964.1:p.Asn34Lys
XM_011510663.1:c.-28C>A XP_011508965.1:n.-28C>A
NM_020989.4:c.102C>A MANE Select NP_066269.1:p.Asn34Lys