Canonical Allele Identifier: CA1426983572
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539570G= , CM000665.2:g.186539570G= GRCh38
NC_000003.11:g.186257359G= , CM000665.1:g.186257359G= GRCh37
NC_000003.10:g.187740053G= NCBI36
NG_009829.1:g.9809C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.49C= MANE Select ENSP00000312099.5:p.Gln17=
ENST00000307944.5:c.49C= ENSP00000312099.5:p.Gln17=
ENST00000392499.6:c.49C= ENSP00000376287.2:p.Gln17=
ENST00000460288.1:n.951C=
NM_017541.2:c.49C= NP_060011.1:p.Gln17=
NM_017541.3:c.49C= NP_060011.1:p.Gln17=
NM_017541.4:c.49C= MANE Select NP_060011.1:p.Gln17=