Canonical Allele Identifier: CA112120805
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs67056118
MyVariant Identifiers: chr4:g.186194267A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194267A>C , CM000666.2:g.186194267A>C GRCh38
NC_000004.11:g.187115421A>C , CM000666.1:g.187115421A>C GRCh37
NC_000004.10:g.187352415A>C NCBI36
NG_007965.1:g.7748A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-233A>C MANE Select ENSP00000368079.4:n.215-233A>C
ENST00000378802.4:c.215-233A>C ENSP00000368079.4:n.215-233A>C
NM_207352.3:c.215-233A>C NP_997235.3:n.215-233A>C
XM_005262935.2:c.215-233A>C XP_005262992.1:n.215-233A>C
XM_005262935.4:c.215-233A>C XP_005262992.1:n.215-233A>C
XM_017008037.1:c.-96-233A>C XP_016863526.1:n.-96-233A>C
NM_207352.4:c.215-233A>C MANE Select NP_997235.3:n.215-233A>C
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