Canonical Allele Identifier: CA670193730
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1049638542
MyVariant Identifiers: chr10:g.96609603A>G (hg19) chr10:g.94849846A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849846A>G , CM000672.2:g.94849846A>G GRCh38
NC_000010.10:g.96609603A>G , CM000672.1:g.96609603A>G GRCh37
NC_000010.9:g.96599593A>G NCBI36
NG_008384.2:g.92141A>G
NG_008384.3:g.92166A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-71A>G MANE Select ENSP00000360372.3:n.1150-71A>G
ENST00000645461.1:n.2061-71A>G
ENST00000371321.7:c.1150-71A>G ENSP00000360372.3:n.1150-71A>G
ENST00000464755.1:c.1913-71A>G ENSP00000483243.1:n.1913-71A>G
NM_000769.2:c.1150-71A>G NP_000760.1:n.1150-71A>G
NM_000769.4:c.1150-71A>G MANE Select NP_000760.1:n.1150-71A>G
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