Canonical Allele Identifier: CA1929278138
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849763T= , CM000672.2:g.94849763T= GRCh38
NC_000010.10:g.96609520T= , CM000672.1:g.96609520T= GRCh37
NC_000010.9:g.96599510T= NCBI36
NG_008384.2:g.92058T=
NG_008384.3:g.92083T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1150-154T= MANE Select ENSP00000360372.3:n.1150-154T=
ENST00000645461.1:n.2061-154T=
ENST00000371321.7:c.1150-154T= ENSP00000360372.3:n.1150-154T=
ENST00000464755.1:c.1913-154T= ENSP00000483243.1:n.1913-154T=
NM_000769.2:c.1150-154T= NP_000760.1:n.1150-154T=
NM_000769.4:c.1150-154T= MANE Select NP_000760.1:n.1150-154T=
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