Canonical Allele Identifier: CA792317631
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1279993910
gnomAD v3: 4-186194438-G-A
gnomAD v4: 4-186194438-G-A
MyVariant Identifiers: chr4:g.187115592G>A (hg19) chr4:g.186194438G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194438G>A , CM000666.2:g.186194438G>A GRCh38
NC_000004.11:g.187115592G>A , CM000666.1:g.187115592G>A GRCh37
NC_000004.10:g.187352586G>A NCBI36
NG_007965.1:g.7919G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-62G>A MANE Select ENSP00000368079.4:n.215-62G>A
ENST00000378802.4:c.215-62G>A ENSP00000368079.4:n.215-62G>A
NM_207352.3:c.215-62G>A NP_997235.3:n.215-62G>A
XM_005262935.2:c.215-62G>A XP_005262992.1:n.215-62G>A
XM_005262935.4:c.215-62G>A XP_005262992.1:n.215-62G>A
XM_017008037.1:c.-96-62G>A XP_016863526.1:n.-96-62G>A
NM_207352.4:c.215-62G>A MANE Select NP_997235.3:n.215-62G>A
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