Canonical Allele Identifier: CA377667863

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1848188150
• MyVariant Identifiers: chr10:g.96522500G>T (hg19) ; chr10:g.94762743G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762743G>T , CM000672.2:g.94762743G>T	GRCh38
NC_000010.10:g.96522500G>T , CM000672.1:g.96522500G>T	GRCh37
NC_000010.9:g.96512490G>T	NCBI36
NG_008384.2:g.5038G>T
NG_008384.3:g.5063G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.38G>T MANE Select	ENSP00000360372.3:p.Cys13Phe
ENST00000371321.7:c.38G>T	ENSP00000360372.3:p.Cys13Phe
ENST00000464755.1:c.932-12315G>T	ENSP00000483243.1:n.932-12315G>T
ENST00000480405.2:c.38G>T	ENSP00000483847.1:p.Cys13Phe
NM_000769.2:c.38G>T	NP_000760.1:p.Cys13Phe
NM_000769.4:c.38G>T MANE Select	NP_000760.1:p.Cys13Phe