Canonical Allele Identifier: CA2672891207
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186201021-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186201021A>C , CM000666.2:g.186201021A>C GRCh38
NC_000004.11:g.187122175A>C , CM000666.1:g.187122175A>C GRCh37
NC_000004.10:g.187359169A>C NCBI36
NG_007965.1:g.14502A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-136A>C MANE Select ENSP00000368079.4:n.802-136A>C
ENST00000378802.4:c.802-136A>C ENSP00000368079.4:n.802-136A>C
ENST00000507209.5:n.1643-136A>C
NM_207352.3:c.802-136A>C NP_997235.3:n.802-136A>C
XM_005262935.2:c.802-136A>C XP_005262992.1:n.802-136A>C
XM_006714184.2:c.406-136A>C XP_006714247.1:n.406-136A>C
XM_005262935.4:c.802-136A>C XP_005262992.1:n.802-136A>C
XM_017008037.1:c.406-136A>C XP_016863526.1:n.406-136A>C
NM_207352.4:c.802-136A>C MANE Select NP_997235.3:n.802-136A>C
Search 100 bp 5'
Search 100 bp 3'