Canonical Allele Identifier: CA358947506
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187118213A>C (hg19) chr4:g.186197059A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197059A>C , CM000666.2:g.186197059A>C GRCh38
NC_000004.11:g.187118213A>C , CM000666.1:g.187118213A>C GRCh37
NC_000004.10:g.187355207A>C NCBI36
NG_007965.1:g.10540A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.533A>C MANE Select ENSP00000368079.4:p.Glu178Ala
ENST00000378802.4:c.533A>C ENSP00000368079.4:p.Glu178Ala
ENST00000507209.5:n.972A>C
NM_207352.3:c.533A>C NP_997235.3:p.Glu178Ala
XM_005262935.2:c.533A>C XP_005262992.1:p.Glu178Ala
XM_006714184.2:c.137A>C XP_006714247.1:p.Glu46Ala
XM_005262935.4:c.533A>C XP_005262992.1:p.Glu178Ala
XM_017008037.1:c.137A>C XP_016863526.1:p.Glu46Ala
NM_207352.4:c.533A>C MANE Select NP_997235.3:p.Glu178Ala
Search 100 bp 5'
Search 100 bp 3'