Canonical Allele Identifier: CA358947567
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1218953078

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197085A>C , CM000666.2:g.186197085A>C GRCh38
NC_000004.11:g.187118239A>C , CM000666.1:g.187118239A>C GRCh37
NC_000004.10:g.187355233A>C NCBI36
NG_007965.1:g.10566A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.559A>C MANE Select ENSP00000368079.4:p.Asn187His
ENST00000378802.4:c.559A>C ENSP00000368079.4:p.Asn187His
ENST00000507209.5:n.998A>C
NM_207352.3:c.559A>C NP_997235.3:p.Asn187His
XM_005262935.2:c.559A>C XP_005262992.1:p.Asn187His
XM_006714184.2:c.163A>C XP_006714247.1:p.Asn55His
XM_005262935.4:c.559A>C XP_005262992.1:p.Asn187His
XM_017008037.1:c.163A>C XP_016863526.1:p.Asn55His
NM_207352.4:c.559A>C MANE Select NP_997235.3:p.Asn187His