Canonical Allele Identifier: CA358946854
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194526A>T , CM000666.2:g.186194526A>T GRCh38
NC_000004.11:g.187115680A>T , CM000666.1:g.187115680A>T GRCh37
NC_000004.10:g.187352674A>T NCBI36
NG_007965.1:g.8007A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.241A>T MANE Select ENSP00000368079.4:p.Thr81Ser
ENST00000378802.4:c.241A>T ENSP00000368079.4:p.Thr81Ser
NM_207352.3:c.241A>T NP_997235.3:p.Thr81Ser
XM_005262935.2:c.241A>T XP_005262992.1:p.Thr81Ser
XM_006714184.2:c.-70A>T XP_006714247.1:n.-70A>T
XM_005262935.4:c.241A>T XP_005262992.1:p.Thr81Ser
XM_017008037.1:c.-70A>T XP_016863526.1:n.-70A>T
NM_207352.4:c.241A>T MANE Select NP_997235.3:p.Thr81Ser