Canonical Allele Identifier: CA670161801
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1459430110
gnomAD v3: 10-94775713-G-A
gnomAD v4: 10-94775713-G-A
MyVariant Identifiers: chr10:g.96535470G>A (hg19) chr10:g.94775713G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775713G>A , CM000672.2:g.94775713G>A GRCh38
NC_000010.10:g.96535470G>A , CM000672.1:g.96535470G>A GRCh37
NC_000010.9:g.96525460G>A NCBI36
NG_008384.2:g.18008G>A
NG_008384.3:g.18033G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+174G>A MANE Select ENSP00000360372.3:n.481+174G>A
ENST00000645461.1:n.1534+174G>A
ENST00000371321.7:c.481+174G>A ENSP00000360372.3:n.481+174G>A
ENST00000464755.1:c.1244+174G>A ENSP00000483243.1:n.1244+174G>A
ENST00000480405.2:c.*166G>A ENSP00000483847.1:n.*166G>A
NM_000769.2:c.481+174G>A NP_000760.1:n.481+174G>A
NM_000769.4:c.481+174G>A MANE Select NP_000760.1:n.481+174G>A
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