Canonical Allele Identifier: CA358946715
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.182G>C MANE Select ENSP00000368079.4:p.Gly61Ala
ENST00000378802.4:c.182G>C ENSP00000368079.4:p.Gly61Ala
NM_207352.3:c.182G>C NP_997235.3:p.Gly61Ala
XM_005262935.2:c.182G>C XP_005262992.1:p.Gly61Ala
XM_005262935.4:c.182G>C XP_005262992.1:p.Gly61Ala
XM_017008037.1:c.-129G>C XP_016863526.1:n.-129G>C
NM_207352.4:c.182G>C MANE Select NP_997235.3:p.Gly61Ala