Canonical Allele Identifier: CA1323928852
Gene: CRYGD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124107C= , CM000664.2:g.208124107C= GRCh38
NC_000002.11:g.208988831C= , CM000664.1:g.208988831C= GRCh37
NC_000002.10:g.208697076C= NCBI36
NG_008039.1:g.5483G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+5G= MANE Select ENSP00000264376.4:n.252+5G=
ENST00000264376.4:c.252+5G= ENSP00000264376.4:n.252+5G=
NM_006891.3:c.252+5G= NP_008822.2:n.252+5G=
NR_038437.1:n.97+4882C=
NM_006891.4:c.252+5G= MANE Select NP_008822.2:n.252+5G=