Canonical Allele Identifier: CA595638678
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1373487771
gnomAD v2: 10-96602582-G-GTGTC
gnomAD v3: 10-94842825-G-GTGTC
gnomAD v4: 10-94842825-G-GTGTC
MyVariant Identifiers: chr10:g.96602582_96602583insTGTC (hg19) chr10:g.94842825_94842826insTGTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842827_94842830dup , CM000672.2:g.94842827_94842830dup GRCh38
NC_000010.10:g.96602584_96602587dup , CM000672.1:g.96602584_96602587dup GRCh37
NC_000010.9:g.96592574_96592577dup NCBI36
NG_008384.2:g.85122_85125dup
NG_008384.3:g.85147_85150dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.962-10_962-7dup MANE Select ENSP00000360372.3:n.962-10_962-7dup
ENST00000645461.1:n.1873-10_1873-7dup
ENST00000371321.7:c.962-10_962-7dup ENSP00000360372.3:n.962-10_962-7dup
ENST00000464755.1:c.1725-10_1725-7dup ENSP00000483243.1:n.1725-10_1725-7dup
NM_000769.2:c.962-10_962-7dup NP_000760.1:n.962-10_962-7dup
NM_000769.4:c.962-10_962-7dup MANE Select NP_000760.1:n.962-10_962-7dup
Search 100 bp 5'
Search 100 bp 3'