Canonical Allele Identifier: CA2672892320
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191820-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191820G>A , CM000666.2:g.186191820G>A GRCh38
NC_000004.11:g.187112974G>A , CM000666.1:g.187112974G>A GRCh37
NC_000004.10:g.187349968G>A NCBI36
NG_007965.1:g.5301G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-4G>A MANE Select ENSP00000368079.4:n.-4G>A
ENST00000378802.4:c.-4G>A ENSP00000368079.4:n.-4G>A
NM_207352.3:c.-4G>A NP_997235.3:n.-4G>A
XM_005262935.2:c.-4G>A XP_005262992.1:n.-4G>A
XM_005262935.4:c.-4G>A XP_005262992.1:n.-4G>A
XM_017008037.1:c.-314G>A XP_016863526.1:n.-314G>A
NM_207352.4:c.-4G>A MANE Select NP_997235.3:n.-4G>A
Search 100 bp 5'
Search 100 bp 3'