Canonical Allele Identifier: CA2672891899
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1388097032
gnomAD v4: 4-186191715-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191715G>A , CM000666.2:g.186191715G>A GRCh38
NC_000004.11:g.187112869G>A , CM000666.1:g.187112869G>A GRCh37
NC_000004.10:g.187349863G>A NCBI36
NG_007965.1:g.5196G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-109G>A MANE Select ENSP00000368079.4:n.-109G>A
ENST00000378802.4:c.-109G>A ENSP00000368079.4:n.-109G>A
NM_207352.3:c.-109G>A NP_997235.3:n.-109G>A
XM_005262935.2:c.-109G>A XP_005262992.1:n.-109G>A
XM_017008037.1:c.-419G>A XP_016863526.1:n.-419G>A
NM_207352.4:c.-109G>A MANE Select NP_997235.3:n.-109G>A
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