Canonical Allele Identifier: CA358946834
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115671A>T (hg19) chr4:g.186194517A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194517A>T , CM000666.2:g.186194517A>T GRCh38
NC_000004.11:g.187115671A>T , CM000666.1:g.187115671A>T GRCh37
NC_000004.10:g.187352665A>T NCBI36
NG_007965.1:g.7998A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.232A>T MANE Select ENSP00000368079.4:p.Ile78Phe
ENST00000378802.4:c.232A>T ENSP00000368079.4:p.Ile78Phe
NM_207352.3:c.232A>T NP_997235.3:p.Ile78Phe
XM_005262935.2:c.232A>T XP_005262992.1:p.Ile78Phe
XM_005262935.4:c.232A>T XP_005262992.1:p.Ile78Phe
XM_017008037.1:c.-79A>T XP_016863526.1:n.-79A>T
NM_207352.4:c.232A>T MANE Select NP_997235.3:p.Ile78Phe
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