Canonical Allele Identifier: CA2077713
Gene: CRYGD HGNC NCBI

Linked Data

dbSNP Id: rs150857132

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124183C>T , CM000664.2:g.208124183C>T GRCh38
NC_000002.11:g.208988907C>T , CM000664.1:g.208988907C>T GRCh37
NC_000002.10:g.208697152C>T NCBI36
NG_008039.1:g.5407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.181G>A MANE Select ENSP00000264376.4:p.Gly61Ser
ENST00000264376.4:c.181G>A ENSP00000264376.4:p.Gly61Ser
NM_006891.3:c.181G>A NP_008822.2:p.Gly61Ser
NR_038437.1:n.97+4958C>T
NM_006891.4:c.181G>A MANE Select NP_008822.2:p.Gly61Ser