Canonical Allele Identifier: CA595638713
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1336469027
gnomAD v2: 10-96612476-TTTG-T
gnomAD v3: 10-94852719-TTTG-T
gnomAD v4: 10-94852719-TTTG-T
MyVariant Identifiers: chr10:g.96612477_96612479del (hg19) chr10:g.94852720_94852722del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852722_94852724del , CM000672.2:g.94852722_94852724del GRCh38
NC_000010.10:g.96612479_96612481del , CM000672.1:g.96612479_96612481del GRCh37
NC_000010.9:g.96602469_96602471del NCBI36
NG_008384.2:g.95017_95019del
NG_008384.3:g.95042_95044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-11_1292-9del MANE Select ENSP00000360372.3:n.1292-11_1292-9del
ENST00000645461.1:n.2203-11_2203-9del
ENST00000371321.7:c.1292-11_1292-9del ENSP00000360372.3:n.1292-11_1292-9del
ENST00000464755.1:c.2055-11_2055-9del ENSP00000483243.1:n.2055-11_2055-9del
NM_000769.2:c.1292-11_1292-9del NP_000760.1:n.1292-11_1292-9del
NM_000769.4:c.1292-11_1292-9del MANE Select NP_000760.1:n.1292-11_1292-9del
Search 100 bp 5'
Search 100 bp 3'