Canonical Allele Identifier: CA1929222244
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781755C= , CM000672.2:g.94781755C= GRCh38
NC_000010.10:g.96541512C= , CM000672.1:g.96541512C= GRCh37
NC_000010.9:g.96531502C= NCBI36
NG_008384.2:g.24050C=
NG_008384.3:g.24075C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-66C= MANE Select ENSP00000360372.3:n.643-66C=
ENST00000645461.1:n.1696-66C=
ENST00000371321.7:c.643-66C= ENSP00000360372.3:n.643-66C=
ENST00000464755.1:c.1406-66C= ENSP00000483243.1:n.1406-66C=
NM_000769.2:c.643-66C= NP_000760.1:n.643-66C=
NM_000769.4:c.643-66C= MANE Select NP_000760.1:n.643-66C=
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