Canonical Allele Identifier: CA112120710
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs535490523
gnomAD v3: 4-186194150-C-G
gnomAD v4: 4-186194150-C-G
MyVariant Identifiers: chr4:g.187115304C>G (hg19) chr4:g.186194150C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194150C>G , CM000666.2:g.186194150C>G GRCh38
NC_000004.11:g.187115304C>G , CM000666.1:g.187115304C>G GRCh37
NC_000004.10:g.187352298C>G NCBI36
NG_007965.1:g.7631C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-350C>G MANE Select ENSP00000368079.4:n.215-350C>G
ENST00000378802.4:c.215-350C>G ENSP00000368079.4:n.215-350C>G
NM_207352.3:c.215-350C>G NP_997235.3:n.215-350C>G
XM_005262935.2:c.215-350C>G XP_005262992.1:n.215-350C>G
XM_005262935.4:c.215-350C>G XP_005262992.1:n.215-350C>G
XM_017008037.1:c.-96-350C>G XP_016863526.1:n.-96-350C>G
NM_207352.4:c.215-350C>G MANE Select NP_997235.3:n.215-350C>G
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