Canonical Allele Identifier: CA5616506
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs200936950

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780665G>A , CM000672.2:g.94780665G>A GRCh38
NC_000010.10:g.96540422G>A , CM000672.1:g.96540422G>A GRCh37
NC_000010.9:g.96530412G>A NCBI36
NG_008384.2:g.22960G>A
NG_008384.3:g.22985G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+6G>A MANE Select ENSP00000360372.3:n.642+6G>A
ENST00000645461.1:n.1695+6G>A
ENST00000371321.7:c.642+6G>A ENSP00000360372.3:n.642+6G>A
ENST00000464755.1:c.1405+6G>A ENSP00000483243.1:n.1405+6G>A
NM_000769.2:c.642+6G>A NP_000760.1:n.642+6G>A
NM_000769.4:c.642+6G>A MANE Select NP_000760.1:n.642+6G>A