Canonical Allele Identifier: CA2672891834
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191698-C-CCCGCAGCGGGGAGCGCGCCAGGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191703_186191725dup , CM000666.2:g.186191703_186191725dup GRCh38
NC_000004.11:g.187112857_187112879dup , CM000666.1:g.187112857_187112879dup GRCh37
NC_000004.10:g.187349851_187349873dup NCBI36
NG_007965.1:g.5184_5206dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-121_-99dup MANE Select ENSP00000368079.4:n.-121_-99dup
ENST00000378802.4:c.-121_-99dup ENSP00000368079.4:n.-121_-99dup
NM_207352.3:c.-121_-99dup NP_997235.3:n.-121_-99dup
XM_005262935.2:c.-121_-99dup XP_005262992.1:n.-121_-99dup
XM_017008037.1:c.-431_-409dup XP_016863526.1:n.-431_-409dup
NM_207352.4:c.-121_-99dup MANE Select NP_997235.3:n.-121_-99dup
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