Canonical Allele Identifier: CA377671303
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs759690171
gnomAD v4: 10-94781890-G-T
MyVariant Identifiers: chr10:g.96541647G>T (hg19) chr10:g.94781890G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781890G>T , CM000672.2:g.94781890G>T GRCh38
NC_000010.10:g.96541647G>T , CM000672.1:g.96541647G>T GRCh37
NC_000010.9:g.96531637G>T NCBI36
NG_008384.2:g.24185G>T
NG_008384.3:g.24210G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.712G>T MANE Select ENSP00000360372.3:p.Ala238Ser
ENST00000645461.1:n.1765G>T
ENST00000371321.7:c.712G>T ENSP00000360372.3:p.Ala238Ser
ENST00000464755.1:c.1475G>T ENSP00000483243.1:n.1475G>T
NM_000769.2:c.712G>T NP_000760.1:p.Ala238Ser
NM_000769.4:c.712G>T MANE Select NP_000760.1:p.Ala238Ser
Search 100 bp 5'
Search 100 bp 3'