Canonical Allele Identifier: CA670193738
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1263766278
MyVariant Identifiers: chr10:g.96609613del (hg19) chr10:g.94849856del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849856del , CM000672.2:g.94849856del GRCh38
NC_000010.10:g.96609613del , CM000672.1:g.96609613del GRCh37
NC_000010.9:g.96599603del NCBI36
NG_008384.2:g.92151del
NG_008384.3:g.92176del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-61del MANE Select ENSP00000360372.3:n.1150-61del
ENST00000645461.1:n.2061-61del
ENST00000371321.7:c.1150-61del ENSP00000360372.3:n.1150-61del
ENST00000464755.1:c.1913-61del ENSP00000483243.1:n.1913-61del
NM_000769.2:c.1150-61del NP_000760.1:n.1150-61del
NM_000769.4:c.1150-61del MANE Select NP_000760.1:n.1150-61del
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