Canonical Allele Identifier: CA1519919030
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197328T= , CM000666.2:g.186197328T= GRCh38
NC_000004.11:g.187118482T= , CM000666.1:g.187118482T= GRCh37
NC_000004.10:g.187355476T= NCBI36
NG_007965.1:g.10809T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+198T= MANE Select ENSP00000368079.4:n.604+198T=
ENST00000378802.4:c.604+198T= ENSP00000368079.4:n.604+198T=
ENST00000507209.5:n.1241T=
NM_207352.3:c.604+198T= NP_997235.3:n.604+198T=
XM_005262935.2:c.604+198T= XP_005262992.1:n.604+198T=
XM_006714184.2:c.208+198T= XP_006714247.1:n.208+198T=
XM_005262935.4:c.604+198T= XP_005262992.1:n.604+198T=
XM_017008037.1:c.208+198T= XP_016863526.1:n.208+198T=
NM_207352.4:c.604+198T= MANE Select NP_997235.3:n.604+198T=