Canonical Allele Identifier: CA5616409
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 39351
ClinVar RCV Id: RCV000394401 RCV000783659
dbSNP Id: rs41291556
ExAC: 10:96535173 T / C
gnomAD v2: 10-96535173-T-C
gnomAD v3: 10-94775416-T-C
gnomAD v4: 10-94775416-T-C
MyVariant Identifiers: chr10:g.96535173T>C (hg19) chr10:g.94775416T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775416T>C , CM000672.2:g.94775416T>C GRCh38
NC_000010.10:g.96535173T>C , CM000672.1:g.96535173T>C GRCh37
NC_000010.9:g.96525163T>C NCBI36
NG_008384.2:g.17711T>C
NG_008384.3:g.17736T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.358T>C MANE Select ENSP00000360372.3:p.Trp120Arg
ENST00000645461.1:n.1411T>C
ENST00000371321.7:c.358T>C ENSP00000360372.3:p.Trp120Arg
ENST00000464755.1:c.1121T>C ENSP00000483243.1:n.1121T>C
ENST00000480405.2:c.358T>C ENSP00000483847.1:p.Trp120Arg
NM_000769.2:c.358T>C NP_000760.1:p.Trp120Arg
NM_000769.4:c.358T>C MANE Select NP_000760.1:p.Trp120Arg
Search 100 bp 5'
Search 100 bp 3'