Canonical Allele Identifier: CA2672891860
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191705-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191705C>T , CM000666.2:g.186191705C>T GRCh38
NC_000004.11:g.187112859C>T , CM000666.1:g.187112859C>T GRCh37
NC_000004.10:g.187349853C>T NCBI36
NG_007965.1:g.5186C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-119C>T MANE Select ENSP00000368079.4:n.-119C>T
ENST00000378802.4:c.-119C>T ENSP00000368079.4:n.-119C>T
NM_207352.3:c.-119C>T NP_997235.3:n.-119C>T
XM_005262935.2:c.-119C>T XP_005262992.1:n.-119C>T
XM_017008037.1:c.-429C>T XP_016863526.1:n.-429C>T
NM_207352.4:c.-119C>T MANE Select NP_997235.3:n.-119C>T
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