Canonical Allele Identifier: CA2672891842
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186191702-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191702C>T , CM000666.2:g.186191702C>T GRCh38
NC_000004.11:g.187112856C>T , CM000666.1:g.187112856C>T GRCh37
NC_000004.10:g.187349850C>T NCBI36
NG_007965.1:g.5183C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-122C>T MANE Select ENSP00000368079.4:n.-122C>T
ENST00000378802.4:c.-122C>T ENSP00000368079.4:n.-122C>T
NM_207352.3:c.-122C>T NP_997235.3:n.-122C>T
XM_005262935.2:c.-122C>T XP_005262992.1:n.-122C>T
XM_017008037.1:c.-432C>T XP_016863526.1:n.-432C>T
NM_207352.4:c.-122C>T MANE Select NP_997235.3:n.-122C>T
Search 100 bp 5'
Search 100 bp 3'