Canonical Allele Identifier: CA1519920408
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs950160125
gnomAD v4: 4-186198898-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198898G>A , CM000666.2:g.186198898G>A GRCh38
NC_000004.11:g.187120052G>A , CM000666.1:g.187120052G>A GRCh37
NC_000004.10:g.187357046G>A NCBI36
NG_007965.1:g.12379G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.675-59G>A MANE Select ENSP00000368079.4:n.675-59G>A
ENST00000378802.4:c.675-59G>A ENSP00000368079.4:n.675-59G>A
ENST00000507209.5:n.1516-59G>A
NM_207352.3:c.675-59G>A NP_997235.3:n.675-59G>A
XM_005262935.2:c.675-59G>A XP_005262992.1:n.675-59G>A
XM_006714184.2:c.279-59G>A XP_006714247.1:n.279-59G>A
XM_005262935.4:c.675-59G>A XP_005262992.1:n.675-59G>A
XM_017008037.1:c.279-59G>A XP_016863526.1:n.279-59G>A
NM_207352.4:c.675-59G>A MANE Select NP_997235.3:n.675-59G>A
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