Canonical Allele Identifier: CA377670567
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780571A>T , CM000672.2:g.94780571A>T GRCh38
NC_000010.10:g.96540328A>T , CM000672.1:g.96540328A>T GRCh37
NC_000010.9:g.96530318A>T NCBI36
NG_008384.2:g.22866A>T
NG_008384.3:g.22891A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.554A>T MANE Select ENSP00000360372.3:p.Lys185Ile
ENST00000371321.7:c.554A>T ENSP00000360372.3:p.Lys185Ile
ENST00000464755.1:n.1317A>T ENSP00000483243.1:p.=
NM_000769.2:c.554A>T NP_000760.1:p.Lys185Ile
NM_000769.4:c.554A>T MANE Select NP_000760.1:p.Lys185Ile