Canonical Allele Identifier: CA437357697
Gene: CRYGS HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.186257270G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539481G>A , CM000665.2:g.186539481G>A GRCh38
NC_000003.11:g.186257270G>A , CM000665.1:g.186257270G>A GRCh37
NC_000003.10:g.187739964G>A NCBI36
NG_009829.1:g.9898C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.138C>T MANE Select ENSP00000312099.5:p.Thr46=
ENST00000307944.5:c.138C>T ENSP00000312099.5:p.Thr46=
ENST00000392499.6:c.138C>T ENSP00000376287.2:p.Thr46=
ENST00000460288.1:n.1040C>T
NM_017541.2:c.138C>T NP_060011.1:p.Thr46=
NM_017541.3:c.138C>T NP_060011.1:p.Thr46=
NM_017541.4:c.138C>T MANE Select NP_060011.1:p.Thr46=
Search 100 bp 5'
Search 100 bp 3'