Canonical Allele Identifier: CA1519891213
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736607058
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208738T>G , CM000666.2:g.186208738T>G GRCh38
NC_000004.11:g.187129892T>G , CM000666.1:g.187129892T>G GRCh37
NC_000004.10:g.187366886T>G NCBI36
NG_007965.1:g.22219T>G
NG_012095.2:g.4760T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1091-127T>G MANE Select ENSP00000368079.4:n.1091-127T>G
ENST00000378802.4:c.1091-127T>G ENSP00000368079.4:n.1091-127T>G
ENST00000502665.1:n.326-127T>G
ENST00000507209.5:n.5789-127T>G
ENST00000513354.5:n.181-127T>G
NM_207352.3:c.1091-127T>G NP_997235.3:n.1091-127T>G
XM_005262935.2:c.1091-127T>G XP_005262992.1:n.1091-127T>G
XM_006714184.2:c.695-127T>G XP_006714247.1:n.695-127T>G
XM_005262935.4:c.1091-127T>G XP_005262992.1:n.1091-127T>G
XM_017008037.1:c.695-127T>G XP_016863526.1:n.695-127T>G
NM_207352.4:c.1091-127T>G MANE Select NP_997235.3:n.1091-127T>G
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