Canonical Allele Identifier: CA211724619
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1002635117
gnomAD v3: 10-94974442-G-T
gnomAD v4: 10-94974442-G-T
MyVariant Identifiers: chr10:g.94974442G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974442G>T , CM000672.2:g.94974442G>T GRCh38
NC_000010.10:g.96734199G>T , CM000672.1:g.96734199G>T GRCh37
NC_000010.9:g.96724189G>T NCBI36
NG_008385.1:g.40785G>T
NG_008385.2:g.41285G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2197G>T MANE Select ENSP00000260682.6:n.961+2197G>T
ENST00000643112.1:c.820-6741G>T ENSP00000496202.1:n.820-6741G>T
ENST00000260682.6:c.961+2197G>T ENSP00000260682.6:n.961+2197G>T
NM_000771.3:c.961+2197G>T NP_000762.2:n.961+2197G>T
NM_000771.4:c.961+2197G>T MANE Select NP_000762.2:n.961+2197G>T
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