Canonical Allele Identifier: CA358946952
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194572C>G , CM000666.2:g.186194572C>G GRCh38
NC_000004.11:g.187115726C>G , CM000666.1:g.187115726C>G GRCh37
NC_000004.10:g.187352720C>G NCBI36
NG_007965.1:g.8053C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.287C>G MANE Select ENSP00000368079.4:p.Pro96Arg
ENST00000378802.4:c.287C>G ENSP00000368079.4:p.Pro96Arg
NM_207352.3:c.287C>G NP_997235.3:p.Pro96Arg
XM_005262935.2:c.287C>G XP_005262992.1:p.Pro96Arg
XM_006714184.2:c.-24C>G XP_006714247.1:n.-24C>G
XM_005262935.4:c.287C>G XP_005262992.1:p.Pro96Arg
XM_017008037.1:c.-24C>G XP_016863526.1:n.-24C>G
NM_207352.4:c.287C>G MANE Select NP_997235.3:p.Pro96Arg