Canonical Allele Identifier: CA442638735
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115745T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194591T>G , CM000666.2:g.186194591T>G GRCh38
NC_000004.11:g.187115745T>G , CM000666.1:g.187115745T>G GRCh37
NC_000004.10:g.187352739T>G NCBI36
NG_007965.1:g.8072T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.306T>G MANE Select ENSP00000368079.4:p.Leu102=
ENST00000378802.4:c.306T>G ENSP00000368079.4:p.Leu102=
NM_207352.3:c.306T>G NP_997235.3:p.Leu102=
XM_005262935.2:c.306T>G XP_005262992.1:p.Leu102=
XM_006714184.2:c.-5T>G XP_006714247.1:n.-5T>G
XM_005262935.4:c.306T>G XP_005262992.1:p.Leu102=
XM_017008037.1:c.-5T>G XP_016863526.1:n.-5T>G
NM_207352.4:c.306T>G MANE Select NP_997235.3:p.Leu102=