Canonical Allele Identifier: CA5616505
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs752599403

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780660G>T , CM000672.2:g.94780660G>T GRCh38
NC_000010.10:g.96540417G>T , CM000672.1:g.96540417G>T GRCh37
NC_000010.9:g.96530407G>T NCBI36
NG_008384.2:g.22955G>T
NG_008384.3:g.22980G>T

Transcript Alleles

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