Canonical Allele Identifier: CA1323928901

Gene: CRYGD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208124189G= , CM000664.2:g.208124189G=	GRCh38
NC_000002.11:g.208988913G= , CM000664.1:g.208988913G=	GRCh37
NC_000002.10:g.208697158G=	NCBI36
NG_008039.1:g.5401C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264376.5:c.175C= MANE Select	ENSP00000264376.4:p.Arg59=
ENST00000264376.4:c.175C=	ENSP00000264376.4:p.Arg59=
NM_006891.3:c.175C=	NP_008822.2:p.Arg59=
NR_038437.1:n.97+4964G=
NM_006891.4:c.175C= MANE Select	NP_008822.2:p.Arg59=