Canonical Allele Identifier: CA377670530
Gene: CYP2C19 HGNC NCBI

Linked Data

COSMIC: COSM122461

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780556C>T , CM000672.2:g.94780556C>T GRCh38
NC_000010.10:g.96540313C>T , CM000672.1:g.96540313C>T GRCh37
NC_000010.9:g.96530303C>T NCBI36
NG_008384.2:g.22851C>T
NG_008384.3:g.22876C>T

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.539C>T NP_000760.1:p.Ser180Phe
NM_000769.4:c.539C>T MANE Select NP_000760.1:p.Ser180Phe
ENST00000371321.7:c.539C>T ENSP00000360372.3:p.Ser180Phe
ENST00000464755.1:n.1302C>T ENSP00000483243.1:p.=