Canonical Allele Identifier: CA211677099
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs17887022
gnomAD v3: 10-94775295-C-A
gnomAD v4: 10-94775295-C-A
MyVariant Identifiers: chr10:g.96535052C>A (hg19) chr10:g.94775295C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775295C>A , CM000672.2:g.94775295C>A GRCh38
NC_000010.10:g.96535052C>A , CM000672.1:g.96535052C>A GRCh37
NC_000010.9:g.96525042C>A NCBI36
NG_008384.2:g.17590C>A
NG_008384.3:g.17615C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.331+75C>A MANE Select ENSP00000360372.3:n.331+75C>A
ENST00000645461.1:n.1384+75C>A
ENST00000371321.7:c.331+75C>A ENSP00000360372.3:n.331+75C>A
ENST00000464755.1:c.1094+75C>A ENSP00000483243.1:n.1094+75C>A
ENST00000480405.2:c.331+75C>A ENSP00000483847.1:n.331+75C>A
NM_000769.2:c.331+75C>A NP_000760.1:n.331+75C>A
NM_000769.4:c.331+75C>A MANE Select NP_000760.1:n.331+75C>A
Search 100 bp 5'
Search 100 bp 3'