Canonical Allele Identifier: CA442640954
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187126389C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205235C>G , CM000666.2:g.186205235C>G GRCh38
NC_000004.11:g.187126389C>G , CM000666.1:g.187126389C>G GRCh37
NC_000004.10:g.187363383C>G NCBI36
NG_007965.1:g.18716C>G
NG_012095.2:g.1257C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1023C>G MANE Select ENSP00000368079.4:p.Ser341=
ENST00000378802.4:c.1023C>G ENSP00000368079.4:p.Ser341=
ENST00000502665.1:n.258C>G
ENST00000507209.5:n.5721C>G
ENST00000513354.5:n.113C>G
NM_207352.3:c.1023C>G NP_997235.3:p.Ser341=
XM_005262935.2:c.1023C>G XP_005262992.1:p.Ser341=
XM_006714184.2:c.627C>G XP_006714247.1:p.Ser209=
XM_005262935.4:c.1023C>G XP_005262992.1:p.Ser341=
XM_017008037.1:c.627C>G XP_016863526.1:p.Ser209=
NM_207352.4:c.1023C>G MANE Select NP_997235.3:p.Ser341=