Canonical Allele Identifier: CA1519919288
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197517C= , CM000666.2:g.186197517C= GRCh38
NC_000004.11:g.187118671C= , CM000666.1:g.187118671C= GRCh37
NC_000004.10:g.187355665C= NCBI36
NG_007965.1:g.10998C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-16C= MANE Select ENSP00000368079.4:n.605-16C=
ENST00000378802.4:c.605-16C= ENSP00000368079.4:n.605-16C=
ENST00000507209.5:n.1430C=
NM_207352.3:c.605-16C= NP_997235.3:n.605-16C=
XM_005262935.2:c.605-16C= XP_005262992.1:n.605-16C=
XM_006714184.2:c.209-16C= XP_006714247.1:n.209-16C=
XM_005262935.4:c.605-16C= XP_005262992.1:n.605-16C=
XM_017008037.1:c.209-16C= XP_016863526.1:n.209-16C=
NM_207352.4:c.605-16C= MANE Select NP_997235.3:n.605-16C=