Canonical Allele Identifier: CA2672891871
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191709G>T , CM000666.2:g.186191709G>T GRCh38
NC_000004.11:g.187112863G>T , CM000666.1:g.187112863G>T GRCh37
NC_000004.10:g.187349857G>T NCBI36
NG_007965.1:g.5190G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-115G>T MANE Select ENSP00000368079.4:n.-115G>T
ENST00000378802.4:c.-115G>T ENSP00000368079.4:n.-115G>T
NM_207352.3:c.-115G>T NP_997235.3:n.-115G>T
XM_005262935.2:c.-115G>T XP_005262992.1:n.-115G>T
XM_017008037.1:c.-425G>T XP_016863526.1:n.-425G>T
NM_207352.4:c.-115G>T MANE Select NP_997235.3:n.-115G>T