Canonical Allele Identifier: CA670193671
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1336750332
gnomAD v3: 10-94849730-T-A
gnomAD v4: 10-94849730-T-A
MyVariant Identifiers: chr10:g.96609487T>A (hg19) chr10:g.94849730T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849730T>A , CM000672.2:g.94849730T>A GRCh38
NC_000010.10:g.96609487T>A , CM000672.1:g.96609487T>A GRCh37
NC_000010.9:g.96599477T>A NCBI36
NG_008384.2:g.92025T>A
NG_008384.3:g.92050T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1150-187T>A MANE Select ENSP00000360372.3:n.1150-187T>A
ENST00000645461.1:n.2061-187T>A
ENST00000371321.7:c.1150-187T>A ENSP00000360372.3:n.1150-187T>A
ENST00000464755.1:c.1913-187T>A ENSP00000483243.1:n.1913-187T>A
NM_000769.2:c.1150-187T>A NP_000760.1:n.1150-187T>A
NM_000769.4:c.1150-187T>A MANE Select NP_000760.1:n.1150-187T>A
Search 100 bp 5'
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