Canonical Allele Identifier: CA1519911082
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192006C= , CM000666.2:g.186192006C= GRCh38
NC_000004.11:g.187113160C= , CM000666.1:g.187113160C= GRCh37
NC_000004.10:g.187350154C= NCBI36
NG_007965.1:g.5487C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.183C= MANE Select ENSP00000368079.4:p.Gly61=
ENST00000378802.4:c.183C= ENSP00000368079.4:p.Gly61=
NM_207352.3:c.183C= NP_997235.3:p.Gly61=
XM_005262935.2:c.183C= XP_005262992.1:p.Gly61=
XM_005262935.4:c.183C= XP_005262992.1:p.Gly61=
XM_017008037.1:c.-128C= XP_016863526.1:n.-128C=
NM_207352.4:c.183C= MANE Select NP_997235.3:p.Gly61=