Canonical Allele Identifier: CA112125034
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1000127688

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197511G>T , CM000666.2:g.186197511G>T GRCh38
NC_000004.11:g.187118665G>T , CM000666.1:g.187118665G>T GRCh37
NC_000004.10:g.187355659G>T NCBI36
NG_007965.1:g.10992G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-22G>T MANE Select ENSP00000368079.4:n.605-22G>T
ENST00000378802.4:c.605-22G>T ENSP00000368079.4:n.605-22G>T
ENST00000507209.5:n.1424G>T
NM_207352.3:c.605-22G>T NP_997235.3:n.605-22G>T
XM_005262935.2:c.605-22G>T XP_005262992.1:n.605-22G>T
XM_006714184.2:c.209-22G>T XP_006714247.1:n.209-22G>T
XM_005262935.4:c.605-22G>T XP_005262992.1:n.605-22G>T
XM_017008037.1:c.209-22G>T XP_016863526.1:n.209-22G>T
NM_207352.4:c.605-22G>T MANE Select NP_997235.3:n.605-22G>T