Canonical Allele Identifier: CA1929279996
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852985A= , CM000672.2:g.94852985A= GRCh38
NC_000010.10:g.96612742A= , CM000672.1:g.96612742A= GRCh37
NC_000010.9:g.96602732A= NCBI36
NG_008384.2:g.95280A=
NG_008384.3:g.95305A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*71A= MANE Select ENSP00000360372.3:n.*71A=
ENST00000645461.1:n.2455A=
ENST00000371321.7:c.*71A= ENSP00000360372.3:n.*71A=
ENST00000464755.1:c.2307A= ENSP00000483243.1:n.2307A=
NM_000769.2:c.*71A= NP_000760.1:n.*71A=
NM_000769.4:c.*71A= MANE Select NP_000760.1:n.*71A=
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