Canonical Allele Identifier: CA1519919497
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197636A= , CM000666.2:g.186197636A= GRCh38
NC_000004.11:g.187118790A= , CM000666.1:g.187118790A= GRCh37
NC_000004.10:g.187355784A= NCBI36
NG_007965.1:g.11117A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.674+34A= MANE Select ENSP00000368079.4:n.674+34A=
ENST00000378802.4:c.674+34A= ENSP00000368079.4:n.674+34A=
ENST00000507209.5:n.1515+34A=
NM_207352.3:c.674+34A= NP_997235.3:n.674+34A=
XM_005262935.2:c.674+34A= XP_005262992.1:n.674+34A=
XM_006714184.2:c.278+34A= XP_006714247.1:n.278+34A=
XM_005262935.4:c.674+34A= XP_005262992.1:n.674+34A=
XM_017008037.1:c.278+34A= XP_016863526.1:n.278+34A=
NM_207352.4:c.674+34A= MANE Select NP_997235.3:n.674+34A=
Search 100 bp 5'
Search 100 bp 3'