Canonical Allele Identifier: CA670165138
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1165986096
gnomAD v3: 10-94781711-C-T
gnomAD v4: 10-94781711-C-T
MyVariant Identifiers: chr10:g.96541468C>T (hg19) chr10:g.94781711C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781711C>T , CM000672.2:g.94781711C>T GRCh38
NC_000010.10:g.96541468C>T , CM000672.1:g.96541468C>T GRCh37
NC_000010.9:g.96531458C>T NCBI36
NG_008384.2:g.24006C>T
NG_008384.3:g.24031C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-110C>T MANE Select ENSP00000360372.3:n.643-110C>T
ENST00000645461.1:n.1696-110C>T
ENST00000371321.7:c.643-110C>T ENSP00000360372.3:n.643-110C>T
ENST00000464755.1:c.1406-110C>T ENSP00000483243.1:n.1406-110C>T
NM_000769.2:c.643-110C>T NP_000760.1:n.643-110C>T
NM_000769.4:c.643-110C>T MANE Select NP_000760.1:n.643-110C>T
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