Canonical Allele Identifier: CA1071986439
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736180732

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197329_186197336dup , CM000666.2:g.186197329_186197336dup GRCh38
NC_000004.11:g.187118483_187118490dup , CM000666.1:g.187118483_187118490dup GRCh37
NC_000004.10:g.187355477_187355484dup NCBI36
NG_007965.1:g.10810_10817dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+199_605-197dup MANE Select ENSP00000368079.4:n.604+199_605-197dup
ENST00000378802.4:c.604+199_605-197dup ENSP00000368079.4:n.604+199_605-197dup
ENST00000507209.5:n.1242_1249dup
NM_207352.3:c.604+199_605-197dup NP_997235.3:n.604+199_605-197dup
XM_005262935.2:c.604+199_605-197dup XP_005262992.1:n.604+199_605-197dup
XM_006714184.2:c.208+199_209-197dup XP_006714247.1:n.208+199_209-197dup
XM_005262935.4:c.604+199_605-197dup XP_005262992.1:n.604+199_605-197dup
XM_017008037.1:c.208+199_209-197dup XP_016863526.1:n.208+199_209-197dup
NM_207352.4:c.604+199_605-197dup MANE Select NP_997235.3:n.604+199_605-197dup