Canonical Allele Identifier: CA1519915364
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194666A= , CM000666.2:g.186194666A= GRCh38
NC_000004.11:g.187115820A= , CM000666.1:g.187115820A= GRCh37
NC_000004.10:g.187352814A= NCBI36
NG_007965.1:g.8147A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.327+54A= MANE Select ENSP00000368079.4:n.327+54A=
ENST00000378802.4:c.327+54A= ENSP00000368079.4:n.327+54A=
NM_207352.3:c.327+54A= NP_997235.3:n.327+54A=
XM_005262935.2:c.327+54A= XP_005262992.1:n.327+54A=
XM_006714184.2:c.17+54A= XP_006714247.1:n.17+54A=
XM_005262935.4:c.327+54A= XP_005262992.1:n.327+54A=
XM_017008037.1:c.17+54A= XP_016863526.1:n.17+54A=
NM_207352.4:c.327+54A= MANE Select NP_997235.3:n.327+54A=