Canonical Allele Identifier: CA3162489
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs772955821

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194564G>A , CM000666.2:g.186194564G>A GRCh38
NC_000004.11:g.187115718G>A , CM000666.1:g.187115718G>A GRCh37
NC_000004.10:g.187352712G>A NCBI36
NG_007965.1:g.8045G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.279G>A MANE Select ENSP00000368079.4:p.Trp93Ter
ENST00000378802.4:c.279G>A ENSP00000368079.4:p.Trp93Ter
NM_207352.3:c.279G>A NP_997235.3:p.Trp93Ter
XM_005262935.2:c.279G>A XP_005262992.1:p.Trp93Ter
XM_006714184.2:c.-32G>A XP_006714247.1:n.-32G>A
XM_005262935.4:c.279G>A XP_005262992.1:p.Trp93Ter
XM_017008037.1:c.-32G>A XP_016863526.1:n.-32G>A
NM_207352.4:c.279G>A MANE Select NP_997235.3:p.Trp93Ter