Canonical Allele Identifier: CA377676389
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96741071A>G (hg19) chr10:g.94981314A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981314A>G , CM000672.2:g.94981314A>G GRCh38
NC_000010.10:g.96741071A>G , CM000672.1:g.96741071A>G GRCh37
NC_000010.9:g.96731061A>G NCBI36
NG_008385.1:g.47657A>G
NG_008385.2:g.48157A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1093A>G MANE Select ENSP00000260682.6:p.Ser365Gly
ENST00000643112.1:c.*102A>G ENSP00000496202.1:n.*102A>G
ENST00000260682.6:c.1093A>G ENSP00000260682.6:p.Ser365Gly
NM_000771.3:c.1093A>G NP_000762.2:p.Ser365Gly
NM_000771.4:c.1093A>G MANE Select NP_000762.2:p.Ser365Gly
Search 100 bp 5'
Search 100 bp 3'