Canonical Allele Identifier: CA2672895518
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186195917-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195917A>T , CM000666.2:g.186195917A>T GRCh38
NC_000004.11:g.187117071A>T , CM000666.1:g.187117071A>T GRCh37
NC_000004.10:g.187354065A>T NCBI36
NG_007965.1:g.9398A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.328-86A>T MANE Select ENSP00000368079.4:n.328-86A>T
ENST00000378802.4:c.328-86A>T ENSP00000368079.4:n.328-86A>T
NM_207352.3:c.328-86A>T NP_997235.3:n.328-86A>T
XM_005262935.2:c.328-86A>T XP_005262992.1:n.328-86A>T
XM_006714184.2:c.18-1023A>T XP_006714247.1:n.18-1023A>T
XM_005262935.4:c.328-86A>T XP_005262992.1:n.328-86A>T
XM_017008037.1:c.18-1023A>T XP_016863526.1:n.18-1023A>T
NM_207352.4:c.328-86A>T MANE Select NP_997235.3:n.328-86A>T
Search 100 bp 5'
Search 100 bp 3'