Canonical Allele Identifier: CA112127471
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1025318513
gnomAD v4: 4-186201096-T-G
MyVariant Identifiers: chr4:g.187122250T>G (hg19) chr4:g.186201096T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186201096T>G , CM000666.2:g.186201096T>G GRCh38
NC_000004.11:g.187122250T>G , CM000666.1:g.187122250T>G GRCh37
NC_000004.10:g.187359244T>G NCBI36
NG_007965.1:g.14577T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-61T>G MANE Select ENSP00000368079.4:n.802-61T>G
ENST00000378802.4:c.802-61T>G ENSP00000368079.4:n.802-61T>G
ENST00000507209.5:n.1643-61T>G
NM_207352.3:c.802-61T>G NP_997235.3:n.802-61T>G
XM_005262935.2:c.802-61T>G XP_005262992.1:n.802-61T>G
XM_006714184.2:c.406-61T>G XP_006714247.1:n.406-61T>G
XM_005262935.4:c.802-61T>G XP_005262992.1:n.802-61T>G
XM_017008037.1:c.406-61T>G XP_016863526.1:n.406-61T>G
NM_207352.4:c.802-61T>G MANE Select NP_997235.3:n.802-61T>G
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