Canonical Allele Identifier: CA2672898192
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186199156-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199156G>A , CM000666.2:g.186199156G>A GRCh38
NC_000004.11:g.187120310G>A , CM000666.1:g.187120310G>A GRCh37
NC_000004.10:g.187357304G>A NCBI36
NG_007965.1:g.12637G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+73G>A MANE Select ENSP00000368079.4:n.801+73G>A
ENST00000378802.4:c.801+73G>A ENSP00000368079.4:n.801+73G>A
ENST00000507209.5:n.1642+73G>A
NM_207352.3:c.801+73G>A NP_997235.3:n.801+73G>A
XM_005262935.2:c.801+73G>A XP_005262992.1:n.801+73G>A
XM_006714184.2:c.405+73G>A XP_006714247.1:n.405+73G>A
XM_005262935.4:c.801+73G>A XP_005262992.1:n.801+73G>A
XM_017008037.1:c.405+73G>A XP_016863526.1:n.405+73G>A
NM_207352.4:c.801+73G>A MANE Select NP_997235.3:n.801+73G>A
Search 100 bp 5'
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