Canonical Allele Identifier: CA470836731
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981319-G-A
MyVariant Identifiers: chr10:g.96741076G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981319G>A , CM000672.2:g.94981319G>A GRCh38
NC_000010.10:g.96741076G>A , CM000672.1:g.96741076G>A GRCh37
NC_000010.9:g.96731066G>A NCBI36
NG_008385.1:g.47662G>A
NG_008385.2:g.48162G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1098G>A MANE Select ENSP00000260682.6:p.Leu366=
ENST00000643112.1:c.*107G>A ENSP00000496202.1:n.*107G>A
ENST00000260682.6:c.1098G>A ENSP00000260682.6:p.Leu366=
NM_000771.3:c.1098G>A NP_000762.2:p.Leu366=
NM_000771.4:c.1098G>A MANE Select NP_000762.2:p.Leu366=
Search 100 bp 5'
Search 100 bp 3'