Canonical Allele Identifier: CA377676018
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96612627G>C (hg19) chr10:g.94852870G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852870G>C , CM000672.2:g.94852870G>C GRCh38
NC_000010.10:g.96612627G>C , CM000672.1:g.96612627G>C GRCh37
NC_000010.9:g.96602617G>C NCBI36
NG_008384.2:g.95165G>C
NG_008384.3:g.95190G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1429G>C MANE Select ENSP00000360372.3:p.Ala477Pro
ENST00000645461.1:n.2340G>C
ENST00000371321.7:c.1429G>C ENSP00000360372.3:p.Ala477Pro
ENST00000464755.1:c.2192G>C ENSP00000483243.1:n.2192G>C
NM_000769.2:c.1429G>C NP_000760.1:p.Ala477Pro
NM_000769.4:c.1429G>C MANE Select NP_000760.1:p.Ala477Pro
Search 100 bp 5'
Search 100 bp 3'