Canonical Allele Identifier: CA350097322
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129584G>C , CM000664.2:g.208129584G>C GRCh38
NC_000002.11:g.208994308G>C , CM000664.1:g.208994308G>C GRCh37
NC_000002.10:g.208702553G>C NCBI36
NG_008038.1:g.5247C>G
NG_008039.1:g.6C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.109C>G MANE Select ENSP00000282141.3:p.Arg37Gly
ENST00000282141.3:c.109C>G ENSP00000282141.3:p.Arg37Gly
NM_020989.3:c.109C>G NP_066269.1:p.Arg37Gly
NR_038437.1:n.98-7472G>C
XM_011510661.1:c.109C>G XP_011508963.1:p.Arg37Gly
XM_011510662.1:c.109C>G XP_011508964.1:p.Arg37Gly
XM_011510663.1:c.-21C>G XP_011508965.1:n.-21C>G
NM_020989.4:c.109C>G MANE Select NP_066269.1:p.Arg37Gly