Canonical Allele Identifier: CA1323928829
Gene: CRYGD HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.208124068T= , CM000664.2:g.208124068T= GRCh38
NC_000002.11:g.208988792T= , CM000664.1:g.208988792T= GRCh37
NC_000002.10:g.208697037T= NCBI36
NG_008039.1:g.5522A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264376.5:c.252+44A= MANE Select ENSP00000264376.4:n.252+44A=
ENST00000264376.4:c.252+44A= ENSP00000264376.4:n.252+44A=
NM_006891.3:c.252+44A= NP_008822.2:n.252+44A=
NR_038437.1:n.97+4843T=
NM_006891.4:c.252+44A= MANE Select NP_008822.2:n.252+44A=
Search 100 bp 5'
Search 100 bp 3'