Canonical Allele Identifier: CA358948145
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199078A>C , CM000666.2:g.186199078A>C GRCh38
NC_000004.11:g.187120232A>C , CM000666.1:g.187120232A>C GRCh37
NC_000004.10:g.187357226A>C NCBI36
NG_007965.1:g.12559A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.796A>C MANE Select ENSP00000368079.4:p.Asn266His
ENST00000378802.4:c.796A>C ENSP00000368079.4:p.Asn266His
ENST00000507209.5:n.1637A>C
NM_207352.3:c.796A>C NP_997235.3:p.Asn266His
XM_005262935.2:c.796A>C XP_005262992.1:p.Asn266His
XM_006714184.2:c.400A>C XP_006714247.1:p.Asn134His
XM_005262935.4:c.796A>C XP_005262992.1:p.Asn266His
XM_017008037.1:c.400A>C XP_016863526.1:p.Asn134His
NM_207352.4:c.796A>C MANE Select NP_997235.3:p.Asn266His