Canonical Allele Identifier: CA3162586
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs569336882
ExAC: 4:187118241 C / G
gnomAD v2: 4-187118241-C-G
gnomAD v3: 4-186197087-C-G
gnomAD v4: 4-186197087-C-G
MyVariant Identifiers: chr4:g.187118241C>G (hg19) chr4:g.186197087C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197087C>G , CM000666.2:g.186197087C>G GRCh38
NC_000004.11:g.187118241C>G , CM000666.1:g.187118241C>G GRCh37
NC_000004.10:g.187355235C>G NCBI36
NG_007965.1:g.10568C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.561C>G MANE Select ENSP00000368079.4:p.Asn187Lys
ENST00000378802.4:c.561C>G ENSP00000368079.4:p.Asn187Lys
ENST00000507209.5:n.1000C>G
NM_207352.3:c.561C>G NP_997235.3:p.Asn187Lys
XM_005262935.2:c.561C>G XP_005262992.1:p.Asn187Lys
XM_006714184.2:c.165C>G XP_006714247.1:p.Asn55Lys
XM_005262935.4:c.561C>G XP_005262992.1:p.Asn187Lys
XM_017008037.1:c.165C>G XP_016863526.1:p.Asn55Lys
NM_207352.4:c.561C>G MANE Select NP_997235.3:p.Asn187Lys
Search 100 bp 5'
Search 100 bp 3'