Canonical Allele Identifier: CA470823799
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96522460T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762703T>G , CM000672.2:g.94762703T>G GRCh38
NC_000010.10:g.96522460T>G , CM000672.1:g.96522460T>G GRCh37
NC_000010.9:g.96512450T>G NCBI36
NG_008384.2:g.4998T>G
NG_008384.3:g.5023T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.-3T>G MANE Select ENSP00000360372.3:n.-3T>G
ENST00000371321.7:c.-3T>G ENSP00000360372.3:n.-3T>G
ENST00000464755.1:c.932-12355T>G ENSP00000483243.1:n.932-12355T>G
ENST00000480405.2:c.-3T>G ENSP00000483847.1:n.-3T>G
NM_000769.2:c.-3T>G NP_000760.1:n.-3T>G
NM_000769.4:c.-3T>G MANE Select NP_000760.1:n.-3T>G
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