Canonical Allele Identifier: CA377668043
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762793C>T , CM000672.2:g.94762793C>T GRCh38
NC_000010.10:g.96522550C>T , CM000672.1:g.96522550C>T GRCh37
NC_000010.9:g.96512540C>T NCBI36
NG_008384.2:g.5088C>T
NG_008384.3:g.5113C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.88C>T MANE Select ENSP00000360372.3:p.Pro30Ser
ENST00000371321.7:c.88C>T ENSP00000360372.3:p.Pro30Ser
ENST00000464755.1:c.932-12265C>T ENSP00000483243.1:n.932-12265C>T
ENST00000480405.2:c.88C>T ENSP00000483847.1:p.Pro30Ser
NM_000769.2:c.88C>T NP_000760.1:p.Pro30Ser
NM_000769.4:c.88C>T MANE Select NP_000760.1:p.Pro30Ser