Canonical Allele Identifier: CA1519910579
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191801C= , CM000666.2:g.186191801C= GRCh38
NC_000004.11:g.187112955C= , CM000666.1:g.187112955C= GRCh37
NC_000004.10:g.187349949C= NCBI36
NG_007965.1:g.5282C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-23C= MANE Select ENSP00000368079.4:n.-23C=
ENST00000378802.4:c.-23C= ENSP00000368079.4:n.-23C=
NM_207352.3:c.-23C= NP_997235.3:n.-23C=
XM_005262935.2:c.-23C= XP_005262992.1:n.-23C=
XM_005262935.4:c.-23C= XP_005262992.1:n.-23C=
XM_017008037.1:c.-333C= XP_016863526.1:n.-333C=
NM_207352.4:c.-23C= MANE Select NP_997235.3:n.-23C=