Canonical Allele Identifier: CA1519919186
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197456T= , CM000666.2:g.186197456T= GRCh38
NC_000004.11:g.187118610T= , CM000666.1:g.187118610T= GRCh37
NC_000004.10:g.187355604T= NCBI36
NG_007965.1:g.10937T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-77T= MANE Select ENSP00000368079.4:n.605-77T=
ENST00000378802.4:c.605-77T= ENSP00000368079.4:n.605-77T=
ENST00000507209.5:n.1369T=
NM_207352.3:c.605-77T= NP_997235.3:n.605-77T=
XM_005262935.2:c.605-77T= XP_005262992.1:n.605-77T=
XM_006714184.2:c.209-77T= XP_006714247.1:n.209-77T=
XM_005262935.4:c.605-77T= XP_005262992.1:n.605-77T=
XM_017008037.1:c.209-77T= XP_016863526.1:n.209-77T=
NM_207352.4:c.605-77T= MANE Select NP_997235.3:n.605-77T=
Search 100 bp 5'
Search 100 bp 3'