Canonical Allele Identifier: CA442883017
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187130422T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209268T>C , CM000666.2:g.186209268T>C GRCh38
NC_000004.11:g.187130422T>C , CM000666.1:g.187130422T>C GRCh37
NC_000004.10:g.187367416T>C NCBI36
NG_007965.1:g.22749T>C
NG_012095.2:g.5290T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1401T>C MANE Select ENSP00000368079.4:p.Cys467=
ENST00000378802.4:c.1401T>C ENSP00000368079.4:p.Cys467=
ENST00000502665.1:n.636T>C
ENST00000507209.5:n.6099T>C
ENST00000511608.5:n.197T>C
ENST00000513354.5:n.491T>C
NM_207352.3:c.1401T>C NP_997235.3:p.Cys467=
XM_005262935.2:c.1398T>C XP_005262992.1:p.Cys466=
XM_006714184.2:c.1005T>C XP_006714247.1:p.Cys335=
XM_005262935.4:c.1398T>C XP_005262992.1:p.Cys466=
XM_017008037.1:c.1005T>C XP_016863526.1:p.Cys335=
NM_207352.4:c.1401T>C MANE Select NP_997235.3:p.Cys467=