Canonical Allele Identifier: CA1426983520
Gene: CRYGS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539470T= , CM000665.2:g.186539470T= GRCh38
NC_000003.11:g.186257259T= , CM000665.1:g.186257259T= GRCh37
NC_000003.10:g.187739953T= NCBI36
NG_009829.1:g.9909A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.149A= MANE Select ENSP00000312099.5:p.Tyr50=
ENST00000307944.5:c.149A= ENSP00000312099.5:p.Tyr50=
ENST00000392499.6:c.149A= ENSP00000376287.2:p.Tyr50=
ENST00000460288.1:n.1051A=
NM_017541.2:c.149A= NP_060011.1:p.Tyr50=
NM_017541.3:c.149A= NP_060011.1:p.Tyr50=
NM_017541.4:c.149A= MANE Select NP_060011.1:p.Tyr50=