Canonical Allele Identifier: CA1519911088
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192009C= , CM000666.2:g.186192009C= GRCh38
NC_000004.11:g.187113163C= , CM000666.1:g.187113163C= GRCh37
NC_000004.10:g.187350157C= NCBI36
NG_007965.1:g.5490C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.186C= MANE Select ENSP00000368079.4:p.His62=
ENST00000378802.4:c.186C= ENSP00000368079.4:p.His62=
NM_207352.3:c.186C= NP_997235.3:p.His62=
XM_005262935.2:c.186C= XP_005262992.1:p.His62=
XM_005262935.4:c.186C= XP_005262992.1:p.His62=
XM_017008037.1:c.-125C= XP_016863526.1:n.-125C=
NM_207352.4:c.186C= MANE Select NP_997235.3:p.His62=