Canonical Allele Identifier: CA557054528
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1219163087

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205151C>T , CM000666.2:g.186205151C>T GRCh38
NC_000004.11:g.187126305C>T , CM000666.1:g.187126305C>T GRCh37
NC_000004.10:g.187363299C>T NCBI36
NG_007965.1:g.18632C>T
NG_012095.2:g.1173C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-49C>T MANE Select ENSP00000368079.4:n.988-49C>T
ENST00000378802.4:c.988-49C>T ENSP00000368079.4:n.988-49C>T
ENST00000502665.1:n.223-49C>T
ENST00000507209.5:n.5637C>T
ENST00000513354.5:n.78-49C>T
NM_207352.3:c.988-49C>T NP_997235.3:n.988-49C>T
XM_005262935.2:c.988-49C>T XP_005262992.1:n.988-49C>T
XM_006714184.2:c.592-49C>T XP_006714247.1:n.592-49C>T
XM_005262935.4:c.988-49C>T XP_005262992.1:n.988-49C>T
XM_017008037.1:c.592-49C>T XP_016863526.1:n.592-49C>T
NM_207352.4:c.988-49C>T MANE Select NP_997235.3:n.988-49C>T