Canonical Allele Identifier: CA1519919014
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197318A= , CM000666.2:g.186197318A= GRCh38
NC_000004.11:g.187118472A= , CM000666.1:g.187118472A= GRCh37
NC_000004.10:g.187355466A= NCBI36
NG_007965.1:g.10799A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+188A= MANE Select ENSP00000368079.4:n.604+188A=
ENST00000378802.4:c.604+188A= ENSP00000368079.4:n.604+188A=
ENST00000507209.5:n.1231A=
NM_207352.3:c.604+188A= NP_997235.3:n.604+188A=
XM_005262935.2:c.604+188A= XP_005262992.1:n.604+188A=
XM_006714184.2:c.208+188A= XP_006714247.1:n.208+188A=
XM_005262935.4:c.604+188A= XP_005262992.1:n.604+188A=
XM_017008037.1:c.208+188A= XP_016863526.1:n.208+188A=
NM_207352.4:c.604+188A= MANE Select NP_997235.3:n.604+188A=