Canonical Allele Identifier: CA377674982
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96609692T>A (hg19) chr10:g.94849935T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849935T>A , CM000672.2:g.94849935T>A GRCh38
NC_000010.10:g.96609692T>A , CM000672.1:g.96609692T>A GRCh37
NC_000010.9:g.96599682T>A NCBI36
NG_008384.2:g.92230T>A
NG_008384.3:g.92255T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1168T>A MANE Select ENSP00000360372.3:p.Ser390Thr
ENST00000645461.1:n.2079T>A
ENST00000371321.7:c.1168T>A ENSP00000360372.3:p.Ser390Thr
ENST00000464755.1:c.1931T>A ENSP00000483243.1:n.1931T>A
NM_000769.2:c.1168T>A NP_000760.1:p.Ser390Thr
NM_000769.4:c.1168T>A MANE Select NP_000760.1:p.Ser390Thr
Search 100 bp 5'
Search 100 bp 3'