Canonical Allele Identifier: CA437357685
Gene: CRYGS HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.186257264A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539475A>C , CM000665.2:g.186539475A>C GRCh38
NC_000003.11:g.186257264A>C , CM000665.1:g.186257264A>C GRCh37
NC_000003.10:g.187739958A>C NCBI36
NG_009829.1:g.9904T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307944.6:c.144T>G MANE Select ENSP00000312099.5:p.Ala48=
ENST00000307944.5:c.144T>G ENSP00000312099.5:p.Ala48=
ENST00000392499.6:c.144T>G ENSP00000376287.2:p.Ala48=
ENST00000460288.1:n.1046T>G
NM_017541.2:c.144T>G NP_060011.1:p.Ala48=
NM_017541.3:c.144T>G NP_060011.1:p.Ala48=
NM_017541.4:c.144T>G MANE Select NP_060011.1:p.Ala48=
Search 100 bp 5'
Search 100 bp 3'