Canonical Allele Identifier: CA470829786

Gene: CYP2C19 MTND4P19

Linked Data

• MyVariant Identifiers: chr10:g.96534271C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94774514C>T , CM000672.2:g.94774514C>T	GRCh38
NC_000010.10:g.96534271C>T , CM000672.1:g.96534271C>T	GRCh37
NC_000010.9:g.96524261C>T	NCBI36
NG_008384.2:g.16809C>T
NG_008384.3:g.16834C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.169-544C>T (CYP2C19) MANE Select	ENSP00000360372.3:n.169-544C>T
ENST00000645461.1:n.678C>T (CYP2C19)
ENST00000371321.7:c.169-544C>T (CYP2C19)	ENSP00000360372.3:n.169-544C>T
ENST00000446659.1:n.120G>A (MTND4P19)
ENST00000464755.1:c.932-544C>T	ENSP00000483243.1:n.932-544C>T
ENST00000480405.2:c.169-544C>T (CYP2C19)	ENSP00000483847.1:n.169-544C>T
NM_000769.2:c.169-544C>T (CYP2C19)	NP_000760.1:n.169-544C>T
NM_000769.4:c.169-544C>T (CYP2C19) MANE Select	NP_000760.1:n.169-544C>T