Canonical Allele Identifier: CA377670548
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780564T>C , CM000672.2:g.94780564T>C GRCh38
NC_000010.10:g.96540321T>C , CM000672.1:g.96540321T>C GRCh37
NC_000010.9:g.96530311T>C NCBI36
NG_008384.2:g.22859T>C
NG_008384.3:g.22884T>C

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.547T>C NP_000760.1:p.Phe183Leu
NM_000769.4:c.547T>C MANE Select NP_000760.1:p.Phe183Leu
ENST00000371321.7:c.547T>C ENSP00000360372.3:p.Phe183Leu
ENST00000464755.1:n.1310T>C ENSP00000483243.1:p.=