Canonical Allele Identifier: CA3162473
Gene: CYP4V2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1626242
ClinVar RCV Id: RCV002132618
dbSNP Id: rs762316724

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194480A>T , CM000666.2:g.186194480A>T GRCh38
NC_000004.11:g.187115634A>T , CM000666.1:g.187115634A>T GRCh37
NC_000004.10:g.187352628A>T NCBI36
NG_007965.1:g.7961A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.215-20A>T MANE Select ENSP00000368079.4:n.215-20A>T
ENST00000378802.4:c.215-20A>T ENSP00000368079.4:n.215-20A>T
NM_207352.3:c.215-20A>T NP_997235.3:n.215-20A>T
XM_005262935.2:c.215-20A>T XP_005262992.1:n.215-20A>T
XM_005262935.4:c.215-20A>T XP_005262992.1:n.215-20A>T
XM_017008037.1:c.-96-20A>T XP_016863526.1:n.-96-20A>T
NM_207352.4:c.215-20A>T MANE Select NP_997235.3:n.215-20A>T