Canonical Allele Identifier: CA1929213983
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762897T= , CM000672.2:g.94762897T= GRCh38
NC_000010.10:g.96522654T= , CM000672.1:g.96522654T= GRCh37
NC_000010.9:g.96512644T= NCBI36
NG_008384.2:g.5192T=
NG_008384.3:g.5217T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.168+24T= MANE Select ENSP00000360372.3:n.168+24T=
ENST00000371321.7:c.168+24T= ENSP00000360372.3:n.168+24T=
ENST00000464755.1:c.932-12161T= ENSP00000483243.1:n.932-12161T=
ENST00000480405.2:c.168+24T= ENSP00000483847.1:n.168+24T=
NM_000769.2:c.168+24T= NP_000760.1:n.168+24T=
NM_000769.4:c.168+24T= MANE Select NP_000760.1:n.168+24T=