Canonical Allele Identifier: CA595638801
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1255287249
gnomAD v2: 10-96701792-G-T
gnomAD v4: 10-94942035-G-T
MyVariant Identifiers: chr10:g.96701792G>T (hg19) chr10:g.94942035G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942035G>T , CM000672.2:g.94942035G>T GRCh38
NC_000010.10:g.96701792G>T , CM000672.1:g.96701792G>T GRCh37
NC_000010.9:g.96691782G>T NCBI36
NG_008385.1:g.8378G>T
NG_008385.2:g.8878G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.331+15G>T MANE Select ENSP00000260682.6:n.331+15G>T
ENST00000643112.1:c.331+15G>T ENSP00000496202.1:n.331+15G>T
ENST00000645207.1:n.484+15G>T
ENST00000260682.6:c.331+15G>T ENSP00000260682.6:n.331+15G>T
ENST00000461906.1:n.356+15G>T
ENST00000473496.1:n.102+15G>T
NM_000771.3:c.331+15G>T NP_000762.2:n.331+15G>T
NM_000771.4:c.331+15G>T MANE Select NP_000762.2:n.331+15G>T
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