Canonical Allele Identifier: CA350097678
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129680T>A , CM000664.2:g.208129680T>A GRCh38
NC_000002.11:g.208994404T>A , CM000664.1:g.208994404T>A GRCh37
NC_000002.10:g.208702649T>A NCBI36
NG_008038.1:g.5151A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.13A>T MANE Select ENSP00000282141.3:p.Thr5Ser
ENST00000282141.3:c.13A>T ENSP00000282141.3:p.Thr5Ser
NM_020989.3:c.13A>T NP_066269.1:p.Thr5Ser
NR_038437.1:n.98-7376T>A
XM_011510661.1:c.13A>T XP_011508963.1:p.Thr5Ser
XM_011510662.1:c.13A>T XP_011508964.1:p.Thr5Ser
XM_011510663.1:c.-117A>T XP_011508965.1:n.-117A>T
NM_020989.4:c.13A>T MANE Select NP_066269.1:p.Thr5Ser