Canonical Allele Identifier: CA377677086
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748720A>G (hg19) chr10:g.94988963A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988963A>G , CM000672.2:g.94988963A>G GRCh38
NC_000010.10:g.96748720A>G , CM000672.1:g.96748720A>G GRCh37
NC_000010.9:g.96738710A>G NCBI36
NG_008385.1:g.55306A>G
NG_008385.2:g.55806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1408A>G MANE Select ENSP00000260682.6:p.Thr470Ala
ENST00000643112.1:c.*417A>G ENSP00000496202.1:n.*417A>G
ENST00000260682.6:c.1408A>G ENSP00000260682.6:p.Thr470Ala
NM_000771.3:c.1408A>G NP_000762.2:p.Thr470Ala
NM_000771.4:c.1408A>G MANE Select NP_000762.2:p.Thr470Ala
Search 100 bp 5'
Search 100 bp 3'