Canonical Allele Identifier: CA442638713
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115724G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194570G>C , CM000666.2:g.186194570G>C GRCh38
NC_000004.11:g.187115724G>C , CM000666.1:g.187115724G>C GRCh37
NC_000004.10:g.187352718G>C NCBI36
NG_007965.1:g.8051G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.285G>C MANE Select ENSP00000368079.4:p.Gly95=
ENST00000378802.4:c.285G>C ENSP00000368079.4:p.Gly95=
NM_207352.3:c.285G>C NP_997235.3:p.Gly95=
XM_005262935.2:c.285G>C XP_005262992.1:p.Gly95=
XM_006714184.2:c.-26G>C XP_006714247.1:p.=
XM_005262935.4:c.285G>C XP_005262992.1:p.Gly95=
XM_017008037.1:c.-26G>C XP_016863526.1:p.=
NM_207352.4:c.285G>C MANE Select NP_997235.3:p.Gly95=