Canonical Allele Identifier: CA437357657
Gene: CRYGS HGNC NCBI

Linked Data

COSMIC: COSM4115933
MyVariant Identifiers: chr3:g.186257252C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539463C>T , CM000665.2:g.186539463C>T GRCh38
NC_000003.11:g.186257252C>T , CM000665.1:g.186257252C>T GRCh37
NC_000003.10:g.187739946C>T NCBI36
NG_009829.1:g.9916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.156G>A MANE Select ENSP00000312099.5:p.Arg52=
ENST00000307944.5:c.156G>A ENSP00000312099.5:p.Arg52=
ENST00000392499.6:c.156G>A ENSP00000376287.2:p.Arg52=
ENST00000460288.1:n.1058G>A
NM_017541.2:c.156G>A NP_060011.1:p.Arg52=
NM_017541.3:c.156G>A NP_060011.1:p.Arg52=
NM_017541.4:c.156G>A MANE Select NP_060011.1:p.Arg52=
Search 100 bp 5'
Search 100 bp 3'