Canonical Allele Identifier: CA377669813
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94775221-G-C
COSMIC: COSM3675928
MyVariant Identifiers: chr10:g.96534978G>C (hg19) chr10:g.94775221G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775221G>C , CM000672.2:g.94775221G>C GRCh38
NC_000010.10:g.96534978G>C , CM000672.1:g.96534978G>C GRCh37
NC_000010.9:g.96524968G>C NCBI36
NG_008384.2:g.17516G>C
NG_008384.3:g.17541G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.331+1G>C MANE Select ENSP00000360372.3:n.331+1G>C
ENST00000645461.1:n.1384+1G>C
ENST00000371321.7:c.331+1G>C ENSP00000360372.3:n.331+1G>C
ENST00000464755.1:c.1094+1G>C ENSP00000483243.1:n.1094+1G>C
ENST00000480405.2:c.331+1G>C ENSP00000483847.1:n.331+1G>C
NM_000769.2:c.331+1G>C NP_000760.1:n.331+1G>C
NM_000769.4:c.331+1G>C MANE Select NP_000760.1:n.331+1G>C
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