Canonical Allele Identifier: CA792319677
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1218432315
MyVariant Identifiers: chr4:g.187118572T>C (hg19) chr4:g.186197418T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197418T>C , CM000666.2:g.186197418T>C GRCh38
NC_000004.11:g.187118572T>C , CM000666.1:g.187118572T>C GRCh37
NC_000004.10:g.187355566T>C NCBI36
NG_007965.1:g.10899T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.605-115T>C MANE Select ENSP00000368079.4:n.605-115T>C
ENST00000378802.4:c.605-115T>C ENSP00000368079.4:n.605-115T>C
ENST00000507209.5:n.1331T>C
NM_207352.3:c.605-115T>C NP_997235.3:n.605-115T>C
XM_005262935.2:c.605-115T>C XP_005262992.1:n.605-115T>C
XM_006714184.2:c.209-115T>C XP_006714247.1:n.209-115T>C
XM_005262935.4:c.605-115T>C XP_005262992.1:n.605-115T>C
XM_017008037.1:c.209-115T>C XP_016863526.1:n.209-115T>C
NM_207352.4:c.605-115T>C MANE Select NP_997235.3:n.605-115T>C
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