Canonical Allele Identifier: CA442638700
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1579961907
MyVariant Identifiers: chr4:g.187115706G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194552G>C , CM000666.2:g.186194552G>C GRCh38
NC_000004.11:g.187115706G>C , CM000666.1:g.187115706G>C GRCh37
NC_000004.10:g.187352700G>C NCBI36
NG_007965.1:g.8033G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.267G>C MANE Select ENSP00000368079.4:p.Leu89=
ENST00000378802.4:c.267G>C ENSP00000368079.4:p.Leu89=
NM_207352.3:c.267G>C NP_997235.3:p.Leu89=
XM_005262935.2:c.267G>C XP_005262992.1:p.Leu89=
XM_006714184.2:c.-44G>C XP_006714247.1:n.-44G>C
XM_005262935.4:c.267G>C XP_005262992.1:p.Leu89=
XM_017008037.1:c.-44G>C XP_016863526.1:n.-44G>C
NM_207352.4:c.267G>C MANE Select NP_997235.3:p.Leu89=
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