Canonical Allele Identifier: CA377670680
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1422071385
gnomAD v2: 10-96540365-G-C
gnomAD v4: 10-94780608-G-C
MyVariant Identifiers: chr10:g.96540365G>C (hg19) chr10:g.94780608G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780608G>C , CM000672.2:g.94780608G>C GRCh38
NC_000010.10:g.96540365G>C , CM000672.1:g.96540365G>C GRCh37
NC_000010.9:g.96530355G>C NCBI36
NG_008384.2:g.22903G>C
NG_008384.3:g.22928G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.591G>C MANE Select ENSP00000360372.3:p.Leu197Phe
ENST00000645461.1:n.1644G>C
ENST00000371321.7:c.591G>C ENSP00000360372.3:p.Leu197Phe
ENST00000464755.1:c.1354G>C ENSP00000483243.1:n.1354G>C
NM_000769.2:c.591G>C NP_000760.1:p.Leu197Phe
NM_000769.4:c.591G>C MANE Select NP_000760.1:p.Leu197Phe
Search 100 bp 5'
Search 100 bp 3'