Canonical Allele Identifier: CA112124508
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs945246638
gnomAD v4: 4-186197077-A-G
MyVariant Identifiers: chr4:g.187118231A>G (hg19) chr4:g.186197077A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197077A>G , CM000666.2:g.186197077A>G GRCh38
NC_000004.11:g.187118231A>G , CM000666.1:g.187118231A>G GRCh37
NC_000004.10:g.187355225A>G NCBI36
NG_007965.1:g.10558A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.551A>G MANE Select ENSP00000368079.4:p.Glu184Gly
ENST00000378802.4:c.551A>G ENSP00000368079.4:p.Glu184Gly
ENST00000507209.5:n.990A>G
NM_207352.3:c.551A>G NP_997235.3:p.Glu184Gly
XM_005262935.2:c.551A>G XP_005262992.1:p.Glu184Gly
XM_006714184.2:c.155A>G XP_006714247.1:p.Glu52Gly
XM_005262935.4:c.551A>G XP_005262992.1:p.Glu184Gly
XM_017008037.1:c.155A>G XP_016863526.1:p.Glu52Gly
NM_207352.4:c.551A>G MANE Select NP_997235.3:p.Glu184Gly
Search 100 bp 5'
Search 100 bp 3'