Canonical Allele Identifier: CA350097340
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129589G>A , CM000664.2:g.208129589G>A GRCh38
NC_000002.11:g.208994313G>A , CM000664.1:g.208994313G>A GRCh37
NC_000002.10:g.208702558G>A NCBI36
NG_008038.1:g.5242C>T
NG_008039.1:g.1C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.104C>T MANE Select ENSP00000282141.3:p.Ser35Phe
ENST00000282141.3:c.104C>T ENSP00000282141.3:p.Ser35Phe
NM_020989.3:c.104C>T NP_066269.1:p.Ser35Phe
NR_038437.1:n.98-7467G>A
XM_011510661.1:c.104C>T XP_011508963.1:p.Ser35Phe
XM_011510662.1:c.104C>T XP_011508964.1:p.Ser35Phe
XM_011510663.1:c.-26C>T XP_011508965.1:n.-26C>T
NM_020989.4:c.104C>T MANE Select NP_066269.1:p.Ser35Phe