Canonical Allele Identifier: CA350097291
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs1574551308

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129575T>C , CM000664.2:g.208129575T>C GRCh38
NC_000002.11:g.208994299T>C , CM000664.1:g.208994299T>C GRCh37
NC_000002.10:g.208702544T>C NCBI36
NG_008038.1:g.5256A>G
NG_008039.1:g.15A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282141.4:c.118A>G MANE Select ENSP00000282141.3:p.Ser40Gly
ENST00000282141.3:c.118A>G ENSP00000282141.3:p.Ser40Gly
NM_020989.3:c.118A>G NP_066269.1:p.Ser40Gly
NR_038437.1:n.98-7481T>C
XM_011510661.1:c.118A>G XP_011508963.1:p.Ser40Gly
XM_011510662.1:c.118A>G XP_011508964.1:p.Ser40Gly
XM_011510663.1:c.-12A>G XP_011508965.1:n.-12A>G
NM_020989.4:c.118A>G MANE Select NP_066269.1:p.Ser40Gly