Canonical Allele Identifier: CA2672898177
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186199104-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199104A>G , CM000666.2:g.186199104A>G GRCh38
NC_000004.11:g.187120258A>G , CM000666.1:g.187120258A>G GRCh37
NC_000004.10:g.187357252A>G NCBI36
NG_007965.1:g.12585A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.801+21A>G MANE Select ENSP00000368079.4:n.801+21A>G
ENST00000378802.4:c.801+21A>G ENSP00000368079.4:n.801+21A>G
ENST00000507209.5:n.1642+21A>G
NM_207352.3:c.801+21A>G NP_997235.3:n.801+21A>G
XM_005262935.2:c.801+21A>G XP_005262992.1:n.801+21A>G
XM_006714184.2:c.405+21A>G XP_006714247.1:n.405+21A>G
XM_005262935.4:c.801+21A>G XP_005262992.1:n.801+21A>G
XM_017008037.1:c.405+21A>G XP_016863526.1:n.405+21A>G
NM_207352.4:c.801+21A>G MANE Select NP_997235.3:n.801+21A>G
Search 100 bp 5'
Search 100 bp 3'