Canonical Allele Identifier: CA1929213975
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762893G= , CM000672.2:g.94762893G= GRCh38
NC_000010.10:g.96522650G= , CM000672.1:g.96522650G= GRCh37
NC_000010.9:g.96512640G= NCBI36
NG_008384.2:g.5188G=
NG_008384.3:g.5213G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.168+20G= MANE Select ENSP00000360372.3:n.168+20G=
ENST00000371321.7:c.168+20G= ENSP00000360372.3:n.168+20G=
ENST00000464755.1:c.932-12165G= ENSP00000483243.1:n.932-12165G=
ENST00000480405.2:c.168+20G= ENSP00000483847.1:n.168+20G=
NM_000769.2:c.168+20G= NP_000760.1:n.168+20G=
NM_000769.4:c.168+20G= MANE Select NP_000760.1:n.168+20G=
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