Canonical Allele Identifier: CA377674987
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1196078753
gnomAD v4: 10-94849936-C-T
COSMIC: COSM3868114
MyVariant Identifiers: chr10:g.96609693C>T (hg19) chr10:g.94849936C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849936C>T , CM000672.2:g.94849936C>T GRCh38
NC_000010.10:g.96609693C>T , CM000672.1:g.96609693C>T GRCh37
NC_000010.9:g.96599683C>T NCBI36
NG_008384.2:g.92231C>T
NG_008384.3:g.92256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1169C>T MANE Select ENSP00000360372.3:p.Ser390Phe
ENST00000645461.1:n.2080C>T
ENST00000371321.7:c.1169C>T ENSP00000360372.3:p.Ser390Phe
ENST00000464755.1:c.1932C>T ENSP00000483243.1:n.1932C>T
NM_000769.2:c.1169C>T NP_000760.1:p.Ser390Phe
NM_000769.4:c.1169C>T MANE Select NP_000760.1:p.Ser390Phe
Search 100 bp 5'
Search 100 bp 3'