Canonical Allele Identifier: CA5616311
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs572853437
ExAC: 10:96522626 C / G
gnomAD v2: 10-96522626-C-G
gnomAD v3: 10-94762869-C-G
gnomAD v4: 10-94762869-C-G
MyVariant Identifiers: chr10:g.96522626C>G (hg19) chr10:g.94762869C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762869C>G , CM000672.2:g.94762869C>G GRCh38
NC_000010.10:g.96522626C>G , CM000672.1:g.96522626C>G GRCh37
NC_000010.9:g.96512616C>G NCBI36
NG_008384.2:g.5164C>G
NG_008384.3:g.5189C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.164C>G MANE Select ENSP00000360372.3:p.Thr55Ser
ENST00000371321.7:c.164C>G ENSP00000360372.3:p.Thr55Ser
ENST00000464755.1:c.932-12189C>G ENSP00000483243.1:n.932-12189C>G
ENST00000480405.2:c.164C>G ENSP00000483847.1:p.Thr55Ser
NM_000769.2:c.164C>G NP_000760.1:p.Thr55Ser
NM_000769.4:c.164C>G MANE Select NP_000760.1:p.Thr55Ser
Search 100 bp 5'
Search 100 bp 3'