Canonical Allele Identifier: CA595321407
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1427756630
gnomAD v2: 10-96535486-T-C
gnomAD v3: 10-94775729-T-C
gnomAD v4: 10-94775729-T-C
MyVariant Identifiers: chr10:g.96535486T>C (hg19) chr10:g.94775729T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775729T>C , CM000672.2:g.94775729T>C GRCh38
NC_000010.10:g.96535486T>C , CM000672.1:g.96535486T>C GRCh37
NC_000010.9:g.96525476T>C NCBI36
NG_008384.2:g.18024T>C
NG_008384.3:g.18049T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+190T>C MANE Select ENSP00000360372.3:n.481+190T>C
ENST00000645461.1:n.1534+190T>C
ENST00000371321.7:c.481+190T>C ENSP00000360372.3:n.481+190T>C
ENST00000464755.1:c.1244+190T>C ENSP00000483243.1:n.1244+190T>C
ENST00000480405.2:c.*182T>C ENSP00000483847.1:n.*182T>C
NM_000769.2:c.481+190T>C NP_000760.1:n.481+190T>C
NM_000769.4:c.481+190T>C MANE Select NP_000760.1:n.481+190T>C
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