Canonical Allele Identifier: CA358946716
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192005G>T , CM000666.2:g.186192005G>T GRCh38
NC_000004.11:g.187113159G>T , CM000666.1:g.187113159G>T GRCh37
NC_000004.10:g.187350153G>T NCBI36
NG_007965.1:g.5486G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.182G>T MANE Select ENSP00000368079.4:p.Gly61Val
ENST00000378802.4:c.182G>T ENSP00000368079.4:p.Gly61Val
NM_207352.3:c.182G>T NP_997235.3:p.Gly61Val
XM_005262935.2:c.182G>T XP_005262992.1:p.Gly61Val
XM_005262935.4:c.182G>T XP_005262992.1:p.Gly61Val
XM_017008037.1:c.-129G>T XP_016863526.1:n.-129G>T
NM_207352.4:c.182G>T MANE Select NP_997235.3:p.Gly61Val