Canonical Allele Identifier: CA2077949
Gene: CRYGC HGNC NCBI

Linked Data

dbSNP Id: rs140859599

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208129583C>T , CM000664.2:g.208129583C>T GRCh38
NC_000002.11:g.208994307C>T , CM000664.1:g.208994307C>T GRCh37
NC_000002.10:g.208702552C>T NCBI36
NG_008038.1:g.5248G>A
NG_008039.1:g.7G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282141.4:c.110G>A MANE Select ENSP00000282141.3:p.Arg37Gln
ENST00000282141.3:c.110G>A ENSP00000282141.3:p.Arg37Gln
NM_020989.3:c.110G>A NP_066269.1:p.Arg37Gln
NR_038437.1:n.98-7473C>T
XM_011510661.1:c.110G>A XP_011508963.1:p.Arg37Gln
XM_011510662.1:c.110G>A XP_011508964.1:p.Arg37Gln
XM_011510663.1:c.-20G>A XP_011508965.1:n.-20G>A
NM_020989.4:c.110G>A MANE Select NP_066269.1:p.Arg37Gln