Canonical Allele Identifier: CA1929213797
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762794C= , CM000672.2:g.94762794C= GRCh38
NC_000010.10:g.96522551C= , CM000672.1:g.96522551C= GRCh37
NC_000010.9:g.96512541C= NCBI36
NG_008384.2:g.5089C=
NG_008384.3:g.5114C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.89C= MANE Select ENSP00000360372.3:p.Pro30=
ENST00000371321.7:c.89C= ENSP00000360372.3:p.Pro30=
ENST00000464755.1:c.932-12264C= ENSP00000483243.1:n.932-12264C=
ENST00000480405.2:c.89C= ENSP00000483847.1:p.Pro30=
NM_000769.2:c.89C= NP_000760.1:p.Pro30=
NM_000769.4:c.89C= MANE Select NP_000760.1:p.Pro30=