Canonical Allele Identifier: CA470987495
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1380656490
gnomAD v4: 10-94775481-T-C
COSMIC: COSM4016870
MyVariant Identifiers: chr10:g.96535238T>C (hg19) chr10:g.94775481T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775481T>C , CM000672.2:g.94775481T>C GRCh38
NC_000010.10:g.96535238T>C , CM000672.1:g.96535238T>C GRCh37
NC_000010.9:g.96525228T>C NCBI36
NG_008384.2:g.17776T>C
NG_008384.3:g.17801T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.423T>C MANE Select ENSP00000360372.3:p.Ile141=
ENST00000645461.1:n.1476T>C
ENST00000371321.7:c.423T>C ENSP00000360372.3:p.Ile141=
ENST00000464755.1:c.1186T>C ENSP00000483243.1:n.1186T>C
ENST00000480405.2:c.423T>C ENSP00000483847.1:p.Ile141=
NM_000769.2:c.423T>C NP_000760.1:p.Ile141=
NM_000769.4:c.423T>C MANE Select NP_000760.1:p.Ile141=
Search 100 bp 5'
Search 100 bp 3'