Canonical Allele Identifier: CA358949877
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208869G>C , CM000666.2:g.186208869G>C GRCh38
NC_000004.11:g.187130023G>C , CM000666.1:g.187130023G>C GRCh37
NC_000004.10:g.187367017G>C NCBI36
NG_007965.1:g.22350G>C
NG_012095.2:g.4891G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1095G>C MANE Select ENSP00000368079.4:p.Lys365Asn
ENST00000378802.4:c.1095G>C ENSP00000368079.4:p.Lys365Asn
ENST00000502665.1:n.330G>C
ENST00000507209.5:n.5793G>C
ENST00000513354.5:n.185G>C
NM_207352.3:c.1095G>C NP_997235.3:p.Lys365Asn
XM_005262935.2:c.1095G>C XP_005262992.1:p.Lys365Asn
XM_006714184.2:c.699G>C XP_006714247.1:p.Lys233Asn
XM_005262935.4:c.1095G>C XP_005262992.1:p.Lys365Asn
XM_017008037.1:c.699G>C XP_016863526.1:p.Lys233Asn
NM_207352.4:c.1095G>C MANE Select NP_997235.3:p.Lys365Asn