Canonical Allele Identifier: CA13249468
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs7918461
gnomAD v2: 10-96522989-A-T
gnomAD v3: 10-94763232-A-T
gnomAD v4: 10-94763232-A-T
MyVariant Identifiers: chr10:g.96522989A>T (hg19) chr10:g.94763232A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94763232A>T , CM000672.2:g.94763232A>T GRCh38
NC_000010.10:g.96522989A>T , CM000672.1:g.96522989A>T GRCh37
NC_000010.9:g.96512979A>T NCBI36
NG_008384.2:g.5527A>T
NG_008384.3:g.5552A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.168+359A>T MANE Select ENSP00000360372.3:n.168+359A>T
ENST00000371321.7:c.168+359A>T ENSP00000360372.3:n.168+359A>T
ENST00000464755.1:c.932-11826A>T ENSP00000483243.1:n.932-11826A>T
ENST00000480405.2:c.168+359A>T ENSP00000483847.1:n.168+359A>T
NM_000769.2:c.168+359A>T NP_000760.1:n.168+359A>T
NM_000769.4:c.168+359A>T MANE Select NP_000760.1:n.168+359A>T
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