Canonical Allele Identifier: CA355704696
Gene: CRYGS HGNC NCBI

Linked Data

dbSNP Id: rs1330606299
gnomAD v2: 3-186257314-T-C
gnomAD v3: 3-186539525-T-C
gnomAD v4: 3-186539525-T-C
MyVariant Identifiers: chr3:g.186257314T>C (hg19) chr3:g.186539525T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186539525T>C , CM000665.2:g.186539525T>C GRCh38
NC_000003.11:g.186257314T>C , CM000665.1:g.186257314T>C GRCh37
NC_000003.10:g.187740008T>C NCBI36
NG_009829.1:g.9854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307944.6:c.94A>G MANE Select ENSP00000312099.5:p.Thr32Ala
ENST00000307944.5:c.94A>G ENSP00000312099.5:p.Thr32Ala
ENST00000392499.6:c.94A>G ENSP00000376287.2:p.Thr32Ala
ENST00000460288.1:n.996A>G
NM_017541.2:c.94A>G NP_060011.1:p.Thr32Ala
NM_017541.3:c.94A>G NP_060011.1:p.Thr32Ala
NM_017541.4:c.94A>G MANE Select NP_060011.1:p.Thr32Ala
Search 100 bp 5'
Search 100 bp 3'