Canonical Allele Identifier: CA377673938
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94949106-A-G
MyVariant Identifiers: chr10:g.96708863A>G (hg19) chr10:g.94949106A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949106A>G , CM000672.2:g.94949106A>G GRCh38
NC_000010.10:g.96708863A>G , CM000672.1:g.96708863A>G GRCh37
NC_000010.9:g.96698853A>G NCBI36
NG_008385.1:g.15449A>G
NG_008385.2:g.15949A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.643-2A>G MANE Select ENSP00000260682.6:n.643-2A>G
ENST00000643112.1:c.643-2A>G ENSP00000496202.1:n.643-2A>G
ENST00000260682.6:c.643-2A>G ENSP00000260682.6:n.643-2A>G
ENST00000473496.1:n.414-2A>G
NM_000771.3:c.643-2A>G NP_000762.2:n.643-2A>G
NM_000771.4:c.643-2A>G MANE Select NP_000762.2:n.643-2A>G
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Search 100 bp 3'