Canonical Allele Identifier: CA442641078
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187130020G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208866G>A , CM000666.2:g.186208866G>A GRCh38
NC_000004.11:g.187130020G>A , CM000666.1:g.187130020G>A GRCh37
NC_000004.10:g.187367014G>A NCBI36
NG_007965.1:g.22347G>A
NG_012095.2:g.4888G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1092G>A MANE Select ENSP00000368079.4:p.Gly364=
ENST00000378802.4:c.1092G>A ENSP00000368079.4:p.Gly364=
ENST00000502665.1:n.327G>A
ENST00000507209.5:n.5790G>A
ENST00000513354.5:n.182G>A
NM_207352.3:c.1092G>A NP_997235.3:p.Gly364=
XM_005262935.2:c.1092G>A XP_005262992.1:p.Gly364=
XM_006714184.2:c.696G>A XP_006714247.1:p.Gly232=
XM_005262935.4:c.1092G>A XP_005262992.1:p.Gly364=
XM_017008037.1:c.696G>A XP_016863526.1:p.Gly232=
NM_207352.4:c.1092G>A MANE Select NP_997235.3:p.Gly364=