Canonical Allele Identifier: CA358948072
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199045A>C , CM000666.2:g.186199045A>C GRCh38
NC_000004.11:g.187120199A>C , CM000666.1:g.187120199A>C GRCh37
NC_000004.10:g.187357193A>C NCBI36
NG_007965.1:g.12526A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.763A>C MANE Select ENSP00000368079.4:p.Lys255Gln
ENST00000378802.4:c.763A>C ENSP00000368079.4:p.Lys255Gln
ENST00000507209.5:n.1604A>C
NM_207352.3:c.763A>C NP_997235.3:p.Lys255Gln
XM_005262935.2:c.763A>C XP_005262992.1:p.Lys255Gln
XM_006714184.2:c.367A>C XP_006714247.1:p.Lys123Gln
XM_005262935.4:c.763A>C XP_005262992.1:p.Lys255Gln
XM_017008037.1:c.367A>C XP_016863526.1:p.Lys123Gln
NM_207352.4:c.763A>C MANE Select NP_997235.3:p.Lys255Gln