Canonical Allele Identifier: CA358947248
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187118098G>C (hg19) chr4:g.186196944G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186196944G>C , CM000666.2:g.186196944G>C GRCh38
NC_000004.11:g.187118098G>C , CM000666.1:g.187118098G>C GRCh37
NC_000004.10:g.187355092G>C NCBI36
NG_007965.1:g.10425G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.418G>C MANE Select ENSP00000368079.4:p.Gly140Arg
ENST00000378802.4:c.418G>C ENSP00000368079.4:p.Gly140Arg
ENST00000507209.5:n.857G>C
NM_207352.3:c.418G>C NP_997235.3:p.Gly140Arg
XM_005262935.2:c.418G>C XP_005262992.1:p.Gly140Arg
XM_006714184.2:c.22G>C XP_006714247.1:p.Gly8Arg
XM_005262935.4:c.418G>C XP_005262992.1:p.Gly140Arg
XM_017008037.1:c.22G>C XP_016863526.1:p.Gly8Arg
NM_207352.4:c.418G>C MANE Select NP_997235.3:p.Gly140Arg
Search 100 bp 5'
Search 100 bp 3'