Canonical Allele Identifier: CA112124931
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs765384088

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197485A>G , CM000666.2:g.186197485A>G GRCh38
NC_000004.11:g.187118639A>G , CM000666.1:g.187118639A>G GRCh37
NC_000004.10:g.187355633A>G NCBI36
NG_007965.1:g.10966A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-48A>G MANE Select ENSP00000368079.4:n.605-48A>G
ENST00000378802.4:c.605-48A>G ENSP00000368079.4:n.605-48A>G
ENST00000507209.5:n.1398A>G
NM_207352.3:c.605-48A>G NP_997235.3:n.605-48A>G
XM_005262935.2:c.605-48A>G XP_005262992.1:n.605-48A>G
XM_006714184.2:c.209-48A>G XP_006714247.1:n.209-48A>G
XM_005262935.4:c.605-48A>G XP_005262992.1:n.605-48A>G
XM_017008037.1:c.209-48A>G XP_016863526.1:n.209-48A>G
NM_207352.4:c.605-48A>G MANE Select NP_997235.3:n.605-48A>G