Canonical Allele Identifier: CA358946965
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194580A>C , CM000666.2:g.186194580A>C GRCh38
NC_000004.11:g.187115734A>C , CM000666.1:g.187115734A>C GRCh37
NC_000004.10:g.187352728A>C NCBI36
NG_007965.1:g.8061A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.295A>C MANE Select ENSP00000368079.4:p.Met99Leu
ENST00000378802.4:c.295A>C ENSP00000368079.4:p.Met99Leu
NM_207352.3:c.295A>C NP_997235.3:p.Met99Leu
XM_005262935.2:c.295A>C XP_005262992.1:p.Met99Leu
XM_006714184.2:c.-16A>C XP_006714247.1:p.=
XM_005262935.4:c.295A>C XP_005262992.1:p.Met99Leu
XM_017008037.1:c.-16A>C XP_016863526.1:p.=
NM_207352.4:c.295A>C MANE Select NP_997235.3:p.Met99Leu