Canonical Allele Identifier: CA2610262448
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762632-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762632T>C , CM000672.2:g.94762632T>C GRCh38
NC_000010.10:g.96522389T>C , CM000672.1:g.96522389T>C GRCh37
NC_000010.9:g.96512379T>C NCBI36
NG_008384.2:g.4927T>C
NG_008384.3:g.4952T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-74T>C ENSP00000360372.3:n.-74T>C
ENST00000464755.1:c.932-12426T>C ENSP00000483243.1:n.932-12426T>C
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