Canonical Allele Identifier: CA112121979
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1026524590
MyVariant Identifiers: chr4:g.187116983A>G (hg19) chr4:g.186195829A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195829A>G , CM000666.2:g.186195829A>G GRCh38
NC_000004.11:g.187116983A>G , CM000666.1:g.187116983A>G GRCh37
NC_000004.10:g.187353977A>G NCBI36
NG_007965.1:g.9310A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.328-174A>G MANE Select ENSP00000368079.4:n.328-174A>G
ENST00000378802.4:c.328-174A>G ENSP00000368079.4:n.328-174A>G
NM_207352.3:c.328-174A>G NP_997235.3:n.328-174A>G
XM_005262935.2:c.328-174A>G XP_005262992.1:n.328-174A>G
XM_006714184.2:c.18-1111A>G XP_006714247.1:n.18-1111A>G
XM_005262935.4:c.328-174A>G XP_005262992.1:n.328-174A>G
XM_017008037.1:c.18-1111A>G XP_016863526.1:n.18-1111A>G
NM_207352.4:c.328-174A>G MANE Select NP_997235.3:n.328-174A>G
Search 100 bp 5'
Search 100 bp 3'