Canonical Allele Identifier: CA670191820
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1175689214
gnomAD v3: 10-94762877-A-C
gnomAD v4: 10-94762877-A-C
MyVariant Identifiers: chr10:g.96522634A>C (hg19) chr10:g.94762877A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762877A>C , CM000672.2:g.94762877A>C GRCh38
NC_000010.10:g.96522634A>C , CM000672.1:g.96522634A>C GRCh37
NC_000010.9:g.96512624A>C NCBI36
NG_008384.2:g.5172A>C
NG_008384.3:g.5197A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.168+4A>C MANE Select ENSP00000360372.3:n.168+4A>C
ENST00000371321.7:c.168+4A>C ENSP00000360372.3:n.168+4A>C
ENST00000464755.1:c.932-12181A>C ENSP00000483243.1:n.932-12181A>C
ENST00000480405.2:c.168+4A>C ENSP00000483847.1:n.168+4A>C
NM_000769.2:c.168+4A>C NP_000760.1:n.168+4A>C
NM_000769.4:c.168+4A>C MANE Select NP_000760.1:n.168+4A>C
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