Canonical Allele Identifier: CA2789070142
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852946T>A , CM000672.2:g.94852946T>A GRCh38
NC_000010.10:g.96612703T>A , CM000672.1:g.96612703T>A GRCh37
NC_000010.9:g.96602693T>A NCBI36
NG_008384.2:g.95241T>A
NG_008384.3:g.95266T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*32T>A MANE Select ENSP00000360372.3:n.*32T>A
ENST00000645461.1:n.2416T>A
ENST00000371321.7:c.*32T>A ENSP00000360372.3:n.*32T>A
ENST00000464755.1:c.2268T>A ENSP00000483243.1:n.2268T>A
NM_000769.2:c.*32T>A NP_000760.1:n.*32T>A
NM_000769.4:c.*32T>A MANE Select NP_000760.1:n.*32T>A
Search 100 bp 5'
Search 100 bp 3'