Canonical Allele Identifier: CA2510109307
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191700-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191700C>A , CM000666.2:g.186191700C>A GRCh38
NC_000004.11:g.187112854C>A , CM000666.1:g.187112854C>A GRCh37
NC_000004.10:g.187349848C>A NCBI36
NG_007965.1:g.5181C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-124C>A MANE Select ENSP00000368079.4:n.-124C>A
ENST00000378802.4:c.-124C>A ENSP00000368079.4:n.-124C>A
NM_207352.3:c.-124C>A NP_997235.3:n.-124C>A
XM_005262935.2:c.-124C>A XP_005262992.1:n.-124C>A
XM_017008037.1:c.-434C>A XP_016863526.1:n.-434C>A
NM_207352.4:c.-124C>A MANE Select NP_997235.3:n.-124C>A
Search 100 bp 5'
Search 100 bp 3'