Canonical Allele Identifier: CA2672891843
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191703-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191703A>C , CM000666.2:g.186191703A>C GRCh38
NC_000004.11:g.187112857A>C , CM000666.1:g.187112857A>C GRCh37
NC_000004.10:g.187349851A>C NCBI36
NG_007965.1:g.5184A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-121A>C MANE Select ENSP00000368079.4:n.-121A>C
ENST00000378802.4:c.-121A>C ENSP00000368079.4:n.-121A>C
NM_207352.3:c.-121A>C NP_997235.3:n.-121A>C
XM_005262935.2:c.-121A>C XP_005262992.1:n.-121A>C
XM_017008037.1:c.-431A>C XP_016863526.1:n.-431A>C
NM_207352.4:c.-121A>C MANE Select NP_997235.3:n.-121A>C
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