Canonical Allele Identifier: CA358946875
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194535T>C , CM000666.2:g.186194535T>C GRCh38
NC_000004.11:g.187115689T>C , CM000666.1:g.187115689T>C GRCh37
NC_000004.10:g.187352683T>C NCBI36
NG_007965.1:g.8016T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.250T>C MANE Select ENSP00000368079.4:p.Tyr84His
ENST00000378802.4:c.250T>C ENSP00000368079.4:p.Tyr84His
NM_207352.3:c.250T>C NP_997235.3:p.Tyr84His
XM_005262935.2:c.250T>C XP_005262992.1:p.Tyr84His
XM_006714184.2:c.-61T>C XP_006714247.1:n.-61T>C
XM_005262935.4:c.250T>C XP_005262992.1:p.Tyr84His
XM_017008037.1:c.-61T>C XP_016863526.1:n.-61T>C
NM_207352.4:c.250T>C MANE Select NP_997235.3:p.Tyr84His