Canonical Allele Identifier: CA112131560
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs372357833

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205159C>G , CM000666.2:g.186205159C>G GRCh38
NC_000004.11:g.187126313C>G , CM000666.1:g.187126313C>G GRCh37
NC_000004.10:g.187363307C>G NCBI36
NG_007965.1:g.18640C>G
NG_012095.2:g.1181C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-41C>G MANE Select ENSP00000368079.4:n.988-41C>G
ENST00000378802.4:c.988-41C>G ENSP00000368079.4:n.988-41C>G
ENST00000502665.1:n.223-41C>G
ENST00000507209.5:n.5645C>G
ENST00000513354.5:n.78-41C>G
NM_207352.3:c.988-41C>G NP_997235.3:n.988-41C>G
XM_005262935.2:c.988-41C>G XP_005262992.1:n.988-41C>G
XM_006714184.2:c.592-41C>G XP_006714247.1:n.592-41C>G
XM_005262935.4:c.988-41C>G XP_005262992.1:n.988-41C>G
XM_017008037.1:c.592-41C>G XP_016863526.1:n.592-41C>G
NM_207352.4:c.988-41C>G MANE Select NP_997235.3:n.988-41C>G