Canonical Allele Identifier: CA595638798
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1188683939
gnomAD v2: 10-96701783-T-C
gnomAD v3: 10-94942026-T-C
gnomAD v4: 10-94942026-T-C
MyVariant Identifiers: chr10:g.96701783T>C (hg19) chr10:g.94942026T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942026T>C , CM000672.2:g.94942026T>C GRCh38
NC_000010.10:g.96701783T>C , CM000672.1:g.96701783T>C GRCh37
NC_000010.9:g.96691773T>C NCBI36
NG_008385.1:g.8369T>C
NG_008385.2:g.8869T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+6T>C MANE Select ENSP00000260682.6:n.331+6T>C
ENST00000643112.1:c.331+6T>C ENSP00000496202.1:n.331+6T>C
ENST00000645207.1:n.484+6T>C
ENST00000260682.6:c.331+6T>C ENSP00000260682.6:n.331+6T>C
ENST00000461906.1:n.356+6T>C
ENST00000473496.1:n.102+6T>C
NM_000771.3:c.331+6T>C NP_000762.2:n.331+6T>C
NM_000771.4:c.331+6T>C MANE Select NP_000762.2:n.331+6T>C
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