Canonical Allele Identifier: CA442638685
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2994673
ClinVar RCV Id: RCV003858296
MyVariant Identifiers: chr4:g.187115697C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194543C>T , CM000666.2:g.186194543C>T GRCh38
NC_000004.11:g.187115697C>T , CM000666.1:g.187115697C>T GRCh37
NC_000004.10:g.187352691C>T NCBI36
NG_007965.1:g.8024C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.258C>T MANE Select ENSP00000368079.4:p.His86=
ENST00000378802.4:c.258C>T ENSP00000368079.4:p.His86=
NM_207352.3:c.258C>T NP_997235.3:p.His86=
XM_005262935.2:c.258C>T XP_005262992.1:p.His86=
XM_006714184.2:c.-53C>T XP_006714247.1:n.-53C>T
XM_005262935.4:c.258C>T XP_005262992.1:p.His86=
XM_017008037.1:c.-53C>T XP_016863526.1:n.-53C>T
NM_207352.4:c.258C>T MANE Select NP_997235.3:p.His86=
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