Canonical Allele Identifier: CA2610263992
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94775538-G-GGGT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775541_94775543dup , CM000672.2:g.94775541_94775543dup GRCh38
NC_000010.10:g.96535298_96535300dup , CM000672.1:g.96535298_96535300dup GRCh37
NC_000010.9:g.96525288_96525290dup NCBI36
NG_008384.2:g.17836_17838dup
NG_008384.3:g.17861_17863dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+2_481+4dup
ENST00000645461.1:n.1534+2_1534+4dup
ENST00000371321.7:c.481+2_481+4dup
ENST00000464755.1:c.1244+2_1244+4dup
ENST00000480405.2:c.483_485dup ENSP00000483847.1:p.Gly162_Ter163insGly
NM_000769.2:c.481+2_481+4dup
NM_000769.4:c.481+2_481+4dup
Search 100 bp 5'
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