Canonical Allele Identifier: CA377671315
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96541651T>C (hg19) chr10:g.94781894T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781894T>C , CM000672.2:g.94781894T>C GRCh38
NC_000010.10:g.96541651T>C , CM000672.1:g.96541651T>C GRCh37
NC_000010.9:g.96531641T>C NCBI36
NG_008384.2:g.24189T>C
NG_008384.3:g.24214T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.716T>C MANE Select ENSP00000360372.3:p.Phe239Ser
ENST00000645461.1:n.1769T>C
ENST00000371321.7:c.716T>C ENSP00000360372.3:p.Phe239Ser
ENST00000464755.1:c.1479T>C ENSP00000483243.1:n.1479T>C
NM_000769.2:c.716T>C NP_000760.1:p.Phe239Ser
NM_000769.4:c.716T>C MANE Select NP_000760.1:p.Phe239Ser
Search 100 bp 5'
Search 100 bp 3'