Canonical Allele Identifier: CA442638699
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186194552-G-A
MyVariant Identifiers: chr4:g.187115706G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194552G>A , CM000666.2:g.186194552G>A GRCh38
NC_000004.11:g.187115706G>A , CM000666.1:g.187115706G>A GRCh37
NC_000004.10:g.187352700G>A NCBI36
NG_007965.1:g.8033G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.267G>A MANE Select ENSP00000368079.4:p.Leu89=
ENST00000378802.4:c.267G>A ENSP00000368079.4:p.Leu89=
NM_207352.3:c.267G>A NP_997235.3:p.Leu89=
XM_005262935.2:c.267G>A XP_005262992.1:p.Leu89=
XM_006714184.2:c.-44G>A XP_006714247.1:n.-44G>A
XM_005262935.4:c.267G>A XP_005262992.1:p.Leu89=
XM_017008037.1:c.-44G>A XP_016863526.1:n.-44G>A
NM_207352.4:c.267G>A MANE Select NP_997235.3:p.Leu89=
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