Canonical Allele Identifier: CA3162607
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1235034
ClinVar RCV Id: RCV001621798
dbSNP Id: rs4862662

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197508G>T , CM000666.2:g.186197508G>T GRCh38
NC_000004.11:g.187118662G>T , CM000666.1:g.187118662G>T GRCh37
NC_000004.10:g.187355656G>T NCBI36
NG_007965.1:g.10989G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-25G>T MANE Select ENSP00000368079.4:n.605-25G>T
ENST00000378802.4:c.605-25G>T ENSP00000368079.4:n.605-25G>T
ENST00000507209.5:n.1421G>T
NM_207352.3:c.605-25G>T NP_997235.3:n.605-25G>T
XM_005262935.2:c.605-25G>T XP_005262992.1:n.605-25G>T
XM_006714184.2:c.209-25G>T XP_006714247.1:n.209-25G>T
XM_005262935.4:c.605-25G>T XP_005262992.1:n.605-25G>T
XM_017008037.1:c.209-25G>T XP_016863526.1:n.209-25G>T
NM_207352.4:c.605-25G>T MANE Select NP_997235.3:n.605-25G>T