Canonical Allele Identifier: CA377675120
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850002T>C , CM000672.2:g.94850002T>C GRCh38
NC_000010.10:g.96609759T>C , CM000672.1:g.96609759T>C GRCh37
NC_000010.9:g.96599749T>C NCBI36
NG_008384.2:g.92297T>C
NG_008384.3:g.92322T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1235T>C MANE Select ENSP00000360372.3:p.Phe412Ser
ENST00000645461.1:n.2146T>C
ENST00000371321.7:c.1235T>C ENSP00000360372.3:p.Phe412Ser
ENST00000464755.1:c.1998T>C ENSP00000483243.1:n.1998T>C
NM_000769.2:c.1235T>C NP_000760.1:p.Phe412Ser
NM_000769.4:c.1235T>C MANE Select NP_000760.1:p.Phe412Ser