Canonical Allele Identifier: CA1929222307

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1848481711
• gnomAD v4: 10-94781805-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781805T>C , CM000672.2:g.94781805T>C	GRCh38
NC_000010.10:g.96541562T>C , CM000672.1:g.96541562T>C	GRCh37
NC_000010.9:g.96531552T>C	NCBI36
NG_008384.2:g.24100T>C
NG_008384.3:g.24125T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.643-16T>C MANE Select	ENSP00000360372.3:n.643-16T>C
ENST00000645461.1:n.1696-16T>C
ENST00000371321.7:c.643-16T>C	ENSP00000360372.3:n.643-16T>C
ENST00000464755.1:c.1406-16T>C	ENSP00000483243.1:n.1406-16T>C
NM_000769.2:c.643-16T>C	NP_000760.1:n.643-16T>C
NM_000769.4:c.643-16T>C MANE Select	NP_000760.1:n.643-16T>C