Canonical Allele Identifier: CA112125881
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs758265175
MyVariant Identifiers: chr4:g.187120030A>C (hg19) chr4:g.186198876A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198876A>C , CM000666.2:g.186198876A>C GRCh38
NC_000004.11:g.187120030A>C , CM000666.1:g.187120030A>C GRCh37
NC_000004.10:g.187357024A>C NCBI36
NG_007965.1:g.12357A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.675-81A>C MANE Select ENSP00000368079.4:n.675-81A>C
ENST00000378802.4:c.675-81A>C ENSP00000368079.4:n.675-81A>C
ENST00000507209.5:n.1516-81A>C
NM_207352.3:c.675-81A>C NP_997235.3:n.675-81A>C
XM_005262935.2:c.675-81A>C XP_005262992.1:n.675-81A>C
XM_006714184.2:c.279-81A>C XP_006714247.1:n.279-81A>C
XM_005262935.4:c.675-81A>C XP_005262992.1:n.675-81A>C
XM_017008037.1:c.279-81A>C XP_016863526.1:n.279-81A>C
NM_207352.4:c.675-81A>C MANE Select NP_997235.3:n.675-81A>C
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