Canonical Allele Identifier: CA442638668
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115655A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194501A>G , CM000666.2:g.186194501A>G GRCh38
NC_000004.11:g.187115655A>G , CM000666.1:g.187115655A>G GRCh37
NC_000004.10:g.187352649A>G NCBI36
NG_007965.1:g.7982A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.216A>G MANE Select ENSP00000368079.4:p.Glu72=
ENST00000378802.4:c.216A>G ENSP00000368079.4:p.Glu72=
NM_207352.3:c.216A>G NP_997235.3:p.Glu72=
XM_005262935.2:c.216A>G XP_005262992.1:p.Glu72=
XM_005262935.4:c.216A>G XP_005262992.1:p.Glu72=
XM_017008037.1:c.-95A>G XP_016863526.1:n.-95A>G
NM_207352.4:c.216A>G MANE Select NP_997235.3:p.Glu72=