Canonical Allele Identifier: CA358947870
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736231523

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198962G>A , CM000666.2:g.186198962G>A GRCh38
NC_000004.11:g.187120116G>A , CM000666.1:g.187120116G>A GRCh37
NC_000004.10:g.187357110G>A NCBI36
NG_007965.1:g.12443G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.680G>A MANE Select ENSP00000368079.4:p.Ser227Asn
ENST00000378802.4:c.680G>A ENSP00000368079.4:p.Ser227Asn
ENST00000507209.5:n.1521G>A
NM_207352.3:c.680G>A NP_997235.3:p.Ser227Asn
XM_005262935.2:c.680G>A XP_005262992.1:p.Ser227Asn
XM_006714184.2:c.284G>A XP_006714247.1:p.Ser95Asn
XM_005262935.4:c.680G>A XP_005262992.1:p.Ser227Asn
XM_017008037.1:c.284G>A XP_016863526.1:p.Ser95Asn
NM_207352.4:c.680G>A MANE Select NP_997235.3:p.Ser227Asn