Canonical Allele Identifier: CA211666287
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1021000556
MyVariant Identifiers: chr10:g.96522491G>C (hg19) chr10:g.94762734G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762734G>C , CM000672.2:g.94762734G>C GRCh38
NC_000010.10:g.96522491G>C , CM000672.1:g.96522491G>C GRCh37
NC_000010.9:g.96512481G>C NCBI36
NG_008384.2:g.5029G>C
NG_008384.3:g.5054G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.29G>C MANE Select ENSP00000360372.3:p.Cys10Ser
ENST00000371321.7:c.29G>C ENSP00000360372.3:p.Cys10Ser
ENST00000464755.1:c.932-12324G>C ENSP00000483243.1:n.932-12324G>C
ENST00000480405.2:c.29G>C ENSP00000483847.1:p.Cys10Ser
NM_000769.2:c.29G>C NP_000760.1:p.Cys10Ser
NM_000769.4:c.29G>C MANE Select NP_000760.1:p.Cys10Ser
Search 100 bp 5'
Search 100 bp 3'