Canonical Allele Identifier: CA112134663
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs921008280

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208852T>C , CM000666.2:g.186208852T>C GRCh38
NC_000004.11:g.187130006T>C , CM000666.1:g.187130006T>C GRCh37
NC_000004.10:g.187367000T>C NCBI36
NG_007965.1:g.22333T>C
NG_012095.2:g.4874T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1091-13T>C MANE Select ENSP00000368079.4:n.1091-13T>C
ENST00000378802.4:c.1091-13T>C ENSP00000368079.4:n.1091-13T>C
ENST00000502665.1:n.326-13T>C
ENST00000507209.5:n.5789-13T>C
ENST00000513354.5:n.181-13T>C
NM_207352.3:c.1091-13T>C NP_997235.3:n.1091-13T>C
XM_005262935.2:c.1091-13T>C XP_005262992.1:n.1091-13T>C
XM_006714184.2:c.695-13T>C XP_006714247.1:n.695-13T>C
XM_005262935.4:c.1091-13T>C XP_005262992.1:n.1091-13T>C
XM_017008037.1:c.695-13T>C XP_016863526.1:n.695-13T>C
NM_207352.4:c.1091-13T>C MANE Select NP_997235.3:n.1091-13T>C