Canonical Allele Identifier: CA2672894779
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186194348-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194348G>A , CM000666.2:g.186194348G>A GRCh38
NC_000004.11:g.187115502G>A , CM000666.1:g.187115502G>A GRCh37
NC_000004.10:g.187352496G>A NCBI36
NG_007965.1:g.7829G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-152G>A MANE Select ENSP00000368079.4:n.215-152G>A
ENST00000378802.4:c.215-152G>A ENSP00000368079.4:n.215-152G>A
NM_207352.3:c.215-152G>A NP_997235.3:n.215-152G>A
XM_005262935.2:c.215-152G>A XP_005262992.1:n.215-152G>A
XM_005262935.4:c.215-152G>A XP_005262992.1:n.215-152G>A
XM_017008037.1:c.-96-152G>A XP_016863526.1:n.-96-152G>A
NM_207352.4:c.215-152G>A MANE Select NP_997235.3:n.215-152G>A
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