Canonical Allele Identifier: CA2672898202
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186199170-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199170T>C , CM000666.2:g.186199170T>C GRCh38
NC_000004.11:g.187120324T>C , CM000666.1:g.187120324T>C GRCh37
NC_000004.10:g.187357318T>C NCBI36
NG_007965.1:g.12651T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.801+87T>C MANE Select ENSP00000368079.4:n.801+87T>C
ENST00000378802.4:c.801+87T>C ENSP00000368079.4:n.801+87T>C
ENST00000507209.5:n.1642+87T>C
NM_207352.3:c.801+87T>C NP_997235.3:n.801+87T>C
XM_005262935.2:c.801+87T>C XP_005262992.1:n.801+87T>C
XM_006714184.2:c.405+87T>C XP_006714247.1:n.405+87T>C
XM_005262935.4:c.801+87T>C XP_005262992.1:n.801+87T>C
XM_017008037.1:c.405+87T>C XP_016863526.1:n.405+87T>C
NM_207352.4:c.801+87T>C MANE Select NP_997235.3:n.801+87T>C
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