Canonical Allele Identifier: CA1323928802
Gene: CRYGD HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124016A= , CM000664.2:g.208124016A= GRCh38
NC_000002.11:g.208988740A= , CM000664.1:g.208988740A= GRCh37
NC_000002.10:g.208696985A= NCBI36
NG_008039.1:g.5574T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+96T= MANE Select ENSP00000264376.4:n.252+96T=
ENST00000264376.4:c.252+96T= ENSP00000264376.4:n.252+96T=
NM_006891.3:c.252+96T= NP_008822.2:n.252+96T=
NR_038437.1:n.97+4791A=
NM_006891.4:c.252+96T= MANE Select NP_008822.2:n.252+96T=
Search 100 bp 5'
Search 100 bp 3'