Canonical Allele Identifier: CA1323931489

Gene: CRYGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129672A= , CM000664.2:g.208129672A=	GRCh38
NC_000002.11:g.208994396A= , CM000664.1:g.208994396A=	GRCh37
NC_000002.10:g.208702641A=	NCBI36
NG_008038.1:g.5159T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.21T= MANE Select	ENSP00000282141.3:p.Tyr7=
ENST00000282141.3:c.21T=	ENSP00000282141.3:p.Tyr7=
NM_020989.3:c.21T=	NP_066269.1:p.Tyr7=
NR_038437.1:n.98-7384A=
XM_011510661.1:c.21T=	XP_011508963.1:p.Tyr7=
XM_011510662.1:c.21T=	XP_011508964.1:p.Tyr7=
XM_011510663.1:c.-109T=	XP_011508965.1:n.-109T=
NM_020989.4:c.21T= MANE Select	NP_066269.1:p.Tyr7=