Canonical Allele Identifier: CA2610266455
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94981156-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981156C>T , CM000672.2:g.94981156C>T GRCh38
NC_000010.10:g.96740913C>T , CM000672.1:g.96740913C>T GRCh37
NC_000010.9:g.96730903C>T NCBI36
NG_008385.1:g.47499C>T
NG_008385.2:g.47999C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-27C>T MANE Select ENSP00000260682.6:n.962-27C>T
ENST00000643112.1:c.820-27C>T ENSP00000496202.1:n.820-27C>T
ENST00000260682.6:c.962-27C>T ENSP00000260682.6:n.962-27C>T
NM_000771.3:c.962-27C>T NP_000762.2:n.962-27C>T
NM_000771.4:c.962-27C>T MANE Select NP_000762.2:n.962-27C>T
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