Canonical Allele Identifier: CA358947698
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187118690C>G (hg19) chr4:g.186197536C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197536C>G , CM000666.2:g.186197536C>G GRCh38
NC_000004.11:g.187118690C>G , CM000666.1:g.187118690C>G GRCh37
NC_000004.10:g.187355684C>G NCBI36
NG_007965.1:g.11017C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.608C>G MANE Select ENSP00000368079.4:p.Thr203Arg
ENST00000378802.4:c.608C>G ENSP00000368079.4:p.Thr203Arg
ENST00000507209.5:n.1449C>G
NM_207352.3:c.608C>G NP_997235.3:p.Thr203Arg
XM_005262935.2:c.608C>G XP_005262992.1:p.Thr203Arg
XM_006714184.2:c.212C>G XP_006714247.1:p.Thr71Arg
XM_005262935.4:c.608C>G XP_005262992.1:p.Thr203Arg
XM_017008037.1:c.212C>G XP_016863526.1:p.Thr71Arg
NM_207352.4:c.608C>G MANE Select NP_997235.3:p.Thr203Arg
Search 100 bp 5'
Search 100 bp 3'