Canonical Allele Identifier: CA211666534
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 769226
ClinVar RCV Id: RCV000948208
dbSNP Id: rs17885098
MyVariant Identifiers: chr10:g.94762804C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762804C>T , CM000672.2:g.94762804C>T GRCh38
NG_008384.2:g.5099C>T
NG_008384.3:g.5124C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.99C>T MANE Select ENSP00000360372.3:p.Pro33=
ENST00000371321.7:c.99C>T ENSP00000360372.3:p.Pro33=
ENST00000464755.1:c.932-12254C>T ENSP00000483243.1:n.932-12254C>T
ENST00000480405.2:c.99C>T ENSP00000483847.1:p.Pro33=
NM_000769.2:c.99C>T NP_000760.1:p.Pro33=
NM_000769.4:c.99C>T MANE Select NP_000760.1:p.Pro33=