Canonical Allele Identifier: CA377670834
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs763055481
gnomAD v2: 10-96540405-C-T
gnomAD v3: 10-94780648-C-T
gnomAD v4: 10-94780648-C-T
COSMIC: COSM5371372
MyVariant Identifiers: chr10:g.96540405C>T (hg19) chr10:g.94780648C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780648C>T , CM000672.2:g.94780648C>T GRCh38
NC_000010.10:g.96540405C>T , CM000672.1:g.96540405C>T GRCh37
NC_000010.9:g.96530395C>T NCBI36
NG_008384.2:g.22943C>T
NG_008384.3:g.22968C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.631C>T MANE Select ENSP00000360372.3:p.Pro211Ser
ENST00000645461.1:n.1684C>T
ENST00000371321.7:c.631C>T ENSP00000360372.3:p.Pro211Ser
ENST00000464755.1:c.1394C>T ENSP00000483243.1:n.1394C>T
NM_000769.2:c.631C>T NP_000760.1:p.Pro211Ser
NM_000769.4:c.631C>T MANE Select NP_000760.1:p.Pro211Ser
Search 100 bp 5'
Search 100 bp 3'