Canonical Allele Identifier: CA437357669
Gene: CRYGS HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.186257258A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539469A>G , CM000665.2:g.186539469A>G GRCh38
NC_000003.11:g.186257258A>G , CM000665.1:g.186257258A>G GRCh37
NC_000003.10:g.187739952A>G NCBI36
NG_009829.1:g.9910T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.150T>C MANE Select ENSP00000312099.5:p.Tyr50=
ENST00000307944.5:c.150T>C ENSP00000312099.5:p.Tyr50=
ENST00000392499.6:c.150T>C ENSP00000376287.2:p.Tyr50=
ENST00000460288.1:n.1052T>C
NM_017541.2:c.150T>C NP_060011.1:p.Tyr50=
NM_017541.3:c.150T>C NP_060011.1:p.Tyr50=
NM_017541.4:c.150T>C MANE Select NP_060011.1:p.Tyr50=
Search 100 bp 5'
Search 100 bp 3'