Canonical Allele Identifier: CA377674988
Gene: CYP2C19 HGNC NCBI

Linked Data

COSMIC: COSM5998952
MyVariant Identifiers: chr10:g.96609695C>A (hg19) chr10:g.94849938C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849938C>A , CM000672.2:g.94849938C>A GRCh38
NC_000010.10:g.96609695C>A , CM000672.1:g.96609695C>A GRCh37
NC_000010.9:g.96599685C>A NCBI36
NG_008384.2:g.92233C>A
NG_008384.3:g.92258C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1171C>A MANE Select ENSP00000360372.3:p.Leu391Ile
ENST00000645461.1:n.2082C>A
ENST00000371321.7:c.1171C>A ENSP00000360372.3:p.Leu391Ile
ENST00000464755.1:c.1934C>A ENSP00000483243.1:n.1934C>A
NM_000769.2:c.1171C>A NP_000760.1:p.Leu391Ile
NM_000769.4:c.1171C>A MANE Select NP_000760.1:p.Leu391Ile
Search 100 bp 5'
Search 100 bp 3'