Canonical Allele Identifier: CA211666188
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs933536968
gnomAD v4: 10-94762678-G-T
MyVariant Identifiers: chr10:g.96522435G>T (hg19) chr10:g.94762678G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762678G>T , CM000672.2:g.94762678G>T GRCh38
NC_000010.10:g.96522435G>T , CM000672.1:g.96522435G>T GRCh37
NC_000010.9:g.96512425G>T NCBI36
NG_008384.2:g.4973G>T
NG_008384.3:g.4998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-28G>T ENSP00000360372.3:n.-28G>T
ENST00000464755.1:c.932-12380G>T ENSP00000483243.1:n.932-12380G>T
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