Canonical Allele Identifier: CA358946859
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736086130

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194529G>C , CM000666.2:g.186194529G>C GRCh38
NC_000004.11:g.187115683G>C , CM000666.1:g.187115683G>C GRCh37
NC_000004.10:g.187352677G>C NCBI36
NG_007965.1:g.8010G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.244G>C MANE Select ENSP00000368079.4:p.Glu82Gln
ENST00000378802.4:c.244G>C ENSP00000368079.4:p.Glu82Gln
NM_207352.3:c.244G>C NP_997235.3:p.Glu82Gln
XM_005262935.2:c.244G>C XP_005262992.1:p.Glu82Gln
XM_006714184.2:c.-67G>C XP_006714247.1:n.-67G>C
XM_005262935.4:c.244G>C XP_005262992.1:p.Glu82Gln
XM_017008037.1:c.-67G>C XP_016863526.1:n.-67G>C
NM_207352.4:c.244G>C MANE Select NP_997235.3:p.Glu82Gln