Canonical Allele Identifier: CA442638687
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115704C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194550C>T , CM000666.2:g.186194550C>T GRCh38
NC_000004.11:g.187115704C>T , CM000666.1:g.187115704C>T GRCh37
NC_000004.10:g.187352698C>T NCBI36
NG_007965.1:g.8031C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.265C>T MANE Select ENSP00000368079.4:p.Leu89=
ENST00000378802.4:c.265C>T ENSP00000368079.4:p.Leu89=
NM_207352.3:c.265C>T NP_997235.3:p.Leu89=
XM_005262935.2:c.265C>T XP_005262992.1:p.Leu89=
XM_006714184.2:c.-46C>T XP_006714247.1:n.-46C>T
XM_005262935.4:c.265C>T XP_005262992.1:p.Leu89=
XM_017008037.1:c.-46C>T XP_016863526.1:n.-46C>T
NM_207352.4:c.265C>T MANE Select NP_997235.3:p.Leu89=
Search 100 bp 5'
Search 100 bp 3'