Canonical Allele Identifier: CA377671250
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94781876-T-C
MyVariant Identifiers: chr10:g.96541633T>C (hg19) chr10:g.94781876T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781876T>C , CM000672.2:g.94781876T>C GRCh38
NC_000010.10:g.96541633T>C , CM000672.1:g.96541633T>C GRCh37
NC_000010.9:g.96531623T>C NCBI36
NG_008384.2:g.24171T>C
NG_008384.3:g.24196T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.698T>C MANE Select ENSP00000360372.3:p.Leu233Ser
ENST00000645461.1:n.1751T>C
ENST00000371321.7:c.698T>C ENSP00000360372.3:p.Leu233Ser
ENST00000464755.1:c.1461T>C ENSP00000483243.1:n.1461T>C
NM_000769.2:c.698T>C NP_000760.1:p.Leu233Ser
NM_000769.4:c.698T>C MANE Select NP_000760.1:p.Leu233Ser
Search 100 bp 5'
Search 100 bp 3'