Canonical Allele Identifier: CA377671321

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96541653A>T (hg19) ; chr10:g.94781896A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781896A>T , CM000672.2:g.94781896A>T	GRCh38
NC_000010.10:g.96541653A>T , CM000672.1:g.96541653A>T	GRCh37
NC_000010.9:g.96531643A>T	NCBI36
NG_008384.2:g.24191A>T
NG_008384.3:g.24216A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.718A>T MANE Select	ENSP00000360372.3:p.Met240Leu
ENST00000645461.1:n.1771A>T
ENST00000371321.7:c.718A>T	ENSP00000360372.3:p.Met240Leu
ENST00000464755.1:c.1481A>T	ENSP00000483243.1:n.1481A>T
NM_000769.2:c.718A>T	NP_000760.1:p.Met240Leu
NM_000769.4:c.718A>T MANE Select	NP_000760.1:p.Met240Leu