Canonical Allele Identifier: CA377670728
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94780620-G-C
MyVariant Identifiers: chr10:g.96540377G>C (hg19) chr10:g.94780620G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780620G>C , CM000672.2:g.94780620G>C GRCh38
NC_000010.10:g.96540377G>C , CM000672.1:g.96540377G>C GRCh37
NC_000010.9:g.96530367G>C NCBI36
NG_008384.2:g.22915G>C
NG_008384.3:g.22940G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.603G>C MANE Select ENSP00000360372.3:p.Leu201Phe
ENST00000645461.1:n.1656G>C
ENST00000371321.7:c.603G>C ENSP00000360372.3:p.Leu201Phe
ENST00000464755.1:c.1366G>C ENSP00000483243.1:n.1366G>C
NM_000769.2:c.603G>C NP_000760.1:p.Leu201Phe
NM_000769.4:c.603G>C MANE Select NP_000760.1:p.Leu201Phe
Search 100 bp 5'
Search 100 bp 3'