Canonical Allele Identifier: CA112118881
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs929171098
MyVariant Identifiers: chr4:g.186191708G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191708G>A , CM000666.2:g.186191708G>A GRCh38
NC_000004.11:g.187112862G>A , CM000666.1:g.187112862G>A GRCh37
NC_000004.10:g.187349856G>A NCBI36
NG_007965.1:g.5189G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.-116G>A MANE Select ENSP00000368079.4:n.-116G>A
ENST00000378802.4:c.-116G>A ENSP00000368079.4:n.-116G>A
NM_207352.3:c.-116G>A NP_997235.3:n.-116G>A
XM_005262935.2:c.-116G>A XP_005262992.1:n.-116G>A
XM_017008037.1:c.-426G>A XP_016863526.1:n.-426G>A
NM_207352.4:c.-116G>A MANE Select NP_997235.3:n.-116G>A
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