Canonical Allele Identifier: CA211735398
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs57749228
gnomAD v2: 10-96748520-G-C
gnomAD v3: 10-94988763-G-C
gnomAD v4: 10-94988763-G-C
MyVariant Identifiers: chr10:g.96748520G>C (hg19) chr10:g.94988763G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988763G>C , CM000672.2:g.94988763G>C GRCh38
NC_000010.10:g.96748520G>C , CM000672.1:g.96748520G>C GRCh37
NC_000010.9:g.96738510G>C NCBI36
NG_008385.1:g.55106G>C
NG_008385.2:g.55606G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1292-84G>C MANE Select ENSP00000260682.6:n.1292-84G>C
ENST00000643112.1:c.*301-84G>C ENSP00000496202.1:n.*301-84G>C
ENST00000260682.6:c.1292-84G>C ENSP00000260682.6:n.1292-84G>C
NM_000771.3:c.1292-84G>C NP_000762.2:n.1292-84G>C
NM_000771.4:c.1292-84G>C MANE Select NP_000762.2:n.1292-84G>C
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