Canonical Allele Identifier: CA595638868
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1336060699
gnomAD v2: 10-96748571-G-A
gnomAD v4: 10-94988814-G-A
MyVariant Identifiers: chr10:g.96748571G>A (hg19) chr10:g.94988814G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988814G>A , CM000672.2:g.94988814G>A GRCh38
NC_000010.10:g.96748571G>A , CM000672.1:g.96748571G>A GRCh37
NC_000010.9:g.96738561G>A NCBI36
NG_008385.1:g.55157G>A
NG_008385.2:g.55657G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-33G>A MANE Select ENSP00000260682.6:n.1292-33G>A
ENST00000643112.1:c.*301-33G>A ENSP00000496202.1:n.*301-33G>A
ENST00000260682.6:c.1292-33G>A ENSP00000260682.6:n.1292-33G>A
NM_000771.3:c.1292-33G>A NP_000762.2:n.1292-33G>A
NM_000771.4:c.1292-33G>A MANE Select NP_000762.2:n.1292-33G>A
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