Canonical Allele Identifier: CA112122037
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs933815019
gnomAD v4: 4-186195957-T-G
MyVariant Identifiers: chr4:g.187117111T>G (hg19) chr4:g.186195957T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195957T>G , CM000666.2:g.186195957T>G GRCh38
NC_000004.11:g.187117111T>G , CM000666.1:g.187117111T>G GRCh37
NC_000004.10:g.187354105T>G NCBI36
NG_007965.1:g.9438T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.328-46T>G MANE Select ENSP00000368079.4:n.328-46T>G
ENST00000378802.4:c.328-46T>G ENSP00000368079.4:n.328-46T>G
NM_207352.3:c.328-46T>G NP_997235.3:n.328-46T>G
XM_005262935.2:c.328-46T>G XP_005262992.1:n.328-46T>G
XM_006714184.2:c.18-983T>G XP_006714247.1:n.18-983T>G
XM_005262935.4:c.328-46T>G XP_005262992.1:n.328-46T>G
XM_017008037.1:c.18-983T>G XP_016863526.1:n.18-983T>G
NM_207352.4:c.328-46T>G MANE Select NP_997235.3:n.328-46T>G
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