Canonical Allele Identifier: CA2518275756
Gene: CYP4V2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208774G>A , CM000666.2:g.186208774G>A GRCh38
NC_000004.11:g.187129928G>A , CM000666.1:g.187129928G>A GRCh37
NC_000004.10:g.187366922G>A NCBI36
NG_007965.1:g.22255G>A
NG_012095.2:g.4796G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1091-91G>A MANE Select ENSP00000368079.4:n.1091-91G>A
ENST00000378802.4:c.1091-91G>A ENSP00000368079.4:n.1091-91G>A
ENST00000502665.1:n.326-91G>A
ENST00000507209.5:n.5789-91G>A
ENST00000513354.5:n.181-91G>A
NM_207352.3:c.1091-91G>A NP_997235.3:n.1091-91G>A
XM_005262935.2:c.1091-91G>A XP_005262992.1:n.1091-91G>A
XM_006714184.2:c.695-91G>A XP_006714247.1:n.695-91G>A
XM_005262935.4:c.1091-91G>A XP_005262992.1:n.1091-91G>A
XM_017008037.1:c.695-91G>A XP_016863526.1:n.695-91G>A
NM_207352.4:c.1091-91G>A MANE Select NP_997235.3:n.1091-91G>A
Search 100 bp 5'
Search 100 bp 3'