Canonical Allele Identifier: CA670165190
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1420068718
gnomAD v4: 10-94781788-CT-C
MyVariant Identifiers: chr10:g.96541546del (hg19) chr10:g.94781789del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781792del , CM000672.2:g.94781792del GRCh38
NC_000010.10:g.96541549del , CM000672.1:g.96541549del GRCh37
NC_000010.9:g.96531539del NCBI36
NG_008384.2:g.24087del
NG_008384.3:g.24112del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.643-29del MANE Select ENSP00000360372.3:n.643-29del
ENST00000645461.1:n.1696-29del
ENST00000371321.7:c.643-29del ENSP00000360372.3:n.643-29del
ENST00000464755.1:c.1406-29del ENSP00000483243.1:n.1406-29del
NM_000769.2:c.643-29del NP_000760.1:n.643-29del
NM_000769.4:c.643-29del MANE Select NP_000760.1:n.643-29del
Search 100 bp 5'
Search 100 bp 3'