Canonical Allele Identifier: CA377671266
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781881A>C , CM000672.2:g.94781881A>C GRCh38
NC_000010.10:g.96541638A>C , CM000672.1:g.96541638A>C GRCh37
NC_000010.9:g.96531628A>C NCBI36
NG_008384.2:g.24176A>C
NG_008384.3:g.24201A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.703A>C MANE Select ENSP00000360372.3:p.Lys235Gln
ENST00000645461.1:n.1756A>C
ENST00000371321.7:c.703A>C ENSP00000360372.3:p.Lys235Gln
ENST00000464755.1:c.1466A>C ENSP00000483243.1:n.1466A>C
NM_000769.2:c.703A>C NP_000760.1:p.Lys235Gln
NM_000769.4:c.703A>C MANE Select NP_000760.1:p.Lys235Gln