Canonical Allele Identifier: CA442882099
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187130110T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208956T>A , CM000666.2:g.186208956T>A GRCh38
NC_000004.11:g.187130110T>A , CM000666.1:g.187130110T>A GRCh37
NC_000004.10:g.187367104T>A NCBI36
NG_007965.1:g.22437T>A
NG_012095.2:g.4978T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1182T>A MANE Select ENSP00000368079.4:p.Ser394=
ENST00000378802.4:c.1182T>A ENSP00000368079.4:p.Ser394=
ENST00000502665.1:n.417T>A
ENST00000507209.5:n.5880T>A
ENST00000513354.5:n.272T>A
NM_207352.3:c.1182T>A NP_997235.3:p.Ser394=
XM_005262935.2:c.1182T>A XP_005262992.1:p.Ser394=
XM_006714184.2:c.786T>A XP_006714247.1:p.Ser262=
XM_005262935.4:c.1182T>A XP_005262992.1:p.Ser394=
XM_017008037.1:c.786T>A XP_016863526.1:p.Ser262=
NM_207352.4:c.1182T>A MANE Select NP_997235.3:p.Ser394=