Canonical Allele Identifier: CA211700598
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs954943263
gnomAD v2: 10-96709071-G-T
gnomAD v3: 10-94949314-G-T
gnomAD v4: 10-94949314-G-T
MyVariant Identifiers: chr10:g.96709071G>T (hg19) chr10:g.94949314G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949314G>T , CM000672.2:g.94949314G>T GRCh38
NC_000010.10:g.96709071G>T , CM000672.1:g.96709071G>T GRCh37
NC_000010.9:g.96699061G>T NCBI36
NG_008385.1:g.15657G>T
NG_008385.2:g.16157G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.819+30G>T MANE Select ENSP00000260682.6:n.819+30G>T
ENST00000643112.1:c.819+30G>T ENSP00000496202.1:n.819+30G>T
ENST00000260682.6:c.819+30G>T ENSP00000260682.6:n.819+30G>T
ENST00000473496.1:n.620G>T
NM_000771.3:c.819+30G>T NP_000762.2:n.819+30G>T
NM_000771.4:c.819+30G>T MANE Select NP_000762.2:n.819+30G>T
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