Canonical Allele Identifier: CA112127456
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1052413571
MyVariant Identifiers: chr4:g.187122149A>C (hg19) chr4:g.186200995A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200995A>C , CM000666.2:g.186200995A>C GRCh38
NC_000004.11:g.187122149A>C , CM000666.1:g.187122149A>C GRCh37
NC_000004.10:g.187359143A>C NCBI36
NG_007965.1:g.14476A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.802-162A>C MANE Select ENSP00000368079.4:n.802-162A>C
ENST00000378802.4:c.802-162A>C ENSP00000368079.4:n.802-162A>C
ENST00000507209.5:n.1643-162A>C
NM_207352.3:c.802-162A>C NP_997235.3:n.802-162A>C
XM_005262935.2:c.802-162A>C XP_005262992.1:n.802-162A>C
XM_006714184.2:c.406-162A>C XP_006714247.1:n.406-162A>C
XM_005262935.4:c.802-162A>C XP_005262992.1:n.802-162A>C
XM_017008037.1:c.406-162A>C XP_016863526.1:n.406-162A>C
NM_207352.4:c.802-162A>C MANE Select NP_997235.3:n.802-162A>C
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