Canonical Allele Identifier: CA431116279
Gene: CRYGC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.208994354A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129630A>G , CM000664.2:g.208129630A>G GRCh38
NC_000002.11:g.208994354A>G , CM000664.1:g.208994354A>G GRCh37
NC_000002.10:g.208702599A>G NCBI36
NG_008038.1:g.5201T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.63T>C MANE Select ENSP00000282141.3:p.Thr21=
ENST00000282141.3:c.63T>C ENSP00000282141.3:p.Thr21=
NM_020989.3:c.63T>C NP_066269.1:p.Thr21=
NR_038437.1:n.98-7426A>G
XM_011510661.1:c.63T>C XP_011508963.1:p.Thr21=
XM_011510662.1:c.63T>C XP_011508964.1:p.Thr21=
XM_011510663.1:c.-67T>C XP_011508965.1:n.-67T>C
NM_020989.4:c.63T>C MANE Select NP_066269.1:p.Thr21=