Canonical Allele Identifier: CA2708144430
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs2126600366
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208774G>C , CM000666.2:g.186208774G>C GRCh38
NC_000004.11:g.187129928G>C , CM000666.1:g.187129928G>C GRCh37
NC_000004.10:g.187366922G>C NCBI36
NG_007965.1:g.22255G>C
NG_012095.2:g.4796G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1091-91G>C MANE Select ENSP00000368079.4:n.1091-91G>C
ENST00000378802.4:c.1091-91G>C ENSP00000368079.4:n.1091-91G>C
ENST00000502665.1:n.326-91G>C
ENST00000507209.5:n.5789-91G>C
ENST00000513354.5:n.181-91G>C
NM_207352.3:c.1091-91G>C NP_997235.3:n.1091-91G>C
XM_005262935.2:c.1091-91G>C XP_005262992.1:n.1091-91G>C
XM_006714184.2:c.695-91G>C XP_006714247.1:n.695-91G>C
XM_005262935.4:c.1091-91G>C XP_005262992.1:n.1091-91G>C
XM_017008037.1:c.695-91G>C XP_016863526.1:n.695-91G>C
NM_207352.4:c.1091-91G>C MANE Select NP_997235.3:n.1091-91G>C
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