Canonical Allele Identifier: CA792321835
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1166301048
MyVariant Identifiers: chr4:g.187122045A>G (hg19) chr4:g.186200891A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200891A>G , CM000666.2:g.186200891A>G GRCh38
NC_000004.11:g.187122045A>G , CM000666.1:g.187122045A>G GRCh37
NC_000004.10:g.187359039A>G NCBI36
NG_007965.1:g.14372A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-266A>G MANE Select ENSP00000368079.4:n.802-266A>G
ENST00000378802.4:c.802-266A>G ENSP00000368079.4:n.802-266A>G
ENST00000507209.5:n.1643-266A>G
NM_207352.3:c.802-266A>G NP_997235.3:n.802-266A>G
XM_005262935.2:c.802-266A>G XP_005262992.1:n.802-266A>G
XM_006714184.2:c.406-266A>G XP_006714247.1:n.406-266A>G
XM_005262935.4:c.802-266A>G XP_005262992.1:n.802-266A>G
XM_017008037.1:c.406-266A>G XP_016863526.1:n.406-266A>G
NM_207352.4:c.802-266A>G MANE Select NP_997235.3:n.802-266A>G
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