Canonical Allele Identifier: CA1519888521
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204798G= , CM000666.2:g.186204798G= GRCh38
NC_000004.11:g.187125952G= , CM000666.1:g.187125952G= GRCh37
NC_000004.10:g.187362946G= NCBI36
NG_007965.1:g.18279G=
NG_012095.2:g.820G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-402G= MANE Select ENSP00000368079.4:n.988-402G=
ENST00000378802.4:c.988-402G= ENSP00000368079.4:n.988-402G=
ENST00000507209.5:n.5284G=
ENST00000513354.5:n.77+341G=
NM_207352.3:c.988-402G= NP_997235.3:n.988-402G=
XM_005262935.2:c.988-402G= XP_005262992.1:n.988-402G=
XM_006714184.2:c.592-402G= XP_006714247.1:n.592-402G=
XM_005262935.4:c.988-402G= XP_005262992.1:n.988-402G=
XM_017008037.1:c.592-402G= XP_016863526.1:n.592-402G=
NM_207352.4:c.988-402G= MANE Select NP_997235.3:n.988-402G=
Search 100 bp 5'
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