Canonical Allele Identifier: CA377671123
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96541596A>C (hg19) chr10:g.94781839A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781839A>C , CM000672.2:g.94781839A>C GRCh38
NC_000010.10:g.96541596A>C , CM000672.1:g.96541596A>C GRCh37
NC_000010.9:g.96531586A>C NCBI36
NG_008384.2:g.24134A>C
NG_008384.3:g.24159A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.661A>C MANE Select ENSP00000360372.3:p.Thr221Pro
ENST00000645461.1:n.1714A>C
ENST00000371321.7:c.661A>C ENSP00000360372.3:p.Thr221Pro
ENST00000464755.1:c.1424A>C ENSP00000483243.1:n.1424A>C
NM_000769.2:c.661A>C NP_000760.1:p.Thr221Pro
NM_000769.4:c.661A>C MANE Select NP_000760.1:p.Thr221Pro
Search 100 bp 5'
Search 100 bp 3'