Canonical Allele Identifier: CA595318369
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1234428213
gnomAD v2: 10-96522431-C-T
gnomAD v4: 10-94762674-C-T
MyVariant Identifiers: chr10:g.96522431C>T (hg19) chr10:g.94762674C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762674C>T , CM000672.2:g.94762674C>T GRCh38
NC_000010.10:g.96522431C>T , CM000672.1:g.96522431C>T GRCh37
NC_000010.9:g.96512421C>T NCBI36
NG_008384.2:g.4969C>T
NG_008384.3:g.4994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-32C>T ENSP00000360372.3:n.-32C>T
ENST00000464755.1:c.932-12384C>T ENSP00000483243.1:n.932-12384C>T
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