Canonical Allele Identifier: CA5616316
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs766303560
ExAC: 10:96522642 CCTT / C
gnomAD v2: 10-96522642-CCTT-C
gnomAD v3: 10-94762885-CCTT-C
gnomAD v4: 10-94762885-CCTT-C
MyVariant Identifiers: chr10:g.96522643_96522645del (hg19) chr10:g.94762886_94762888del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762887_94762889del , CM000672.2:g.94762887_94762889del GRCh38
NC_000010.10:g.96522644_96522646del , CM000672.1:g.96522644_96522646del GRCh37
NC_000010.9:g.96512634_96512636del NCBI36
NG_008384.2:g.5182_5184del
NG_008384.3:g.5207_5209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.168+14_168+16del MANE Select ENSP00000360372.3:n.168+14_168+16del
ENST00000371321.7:c.168+14_168+16del ENSP00000360372.3:n.168+14_168+16del
ENST00000464755.1:c.932-12171_932-12169del ENSP00000483243.1:n.932-12171_932-12169del
ENST00000480405.2:c.168+14_168+16del ENSP00000483847.1:n.168+14_168+16del
NM_000769.2:c.168+14_168+16del NP_000760.1:n.168+14_168+16del
NM_000769.4:c.168+14_168+16del MANE Select NP_000760.1:n.168+14_168+16del
Search 100 bp 5'
Search 100 bp 3'