Canonical Allele Identifier: CA470832887
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849626845
gnomAD v3: 10-94849946-T-G
gnomAD v4: 10-94849946-T-G
MyVariant Identifiers: chr10:g.96609703T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849946T>G , CM000672.2:g.94849946T>G GRCh38
NC_000010.10:g.96609703T>G , CM000672.1:g.96609703T>G GRCh37
NC_000010.9:g.96599693T>G NCBI36
NG_008384.2:g.92241T>G
NG_008384.3:g.92266T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1179T>G MANE Select ENSP00000360372.3:p.Ser393=
ENST00000645461.1:n.2090T>G
ENST00000371321.7:c.1179T>G ENSP00000360372.3:p.Ser393=
ENST00000464755.1:c.1942T>G ENSP00000483243.1:n.1942T>G
NM_000769.2:c.1179T>G NP_000760.1:p.Ser393=
NM_000769.4:c.1179T>G MANE Select NP_000760.1:p.Ser393=
Search 100 bp 5'
Search 100 bp 3'