Canonical Allele Identifier: CA358947645
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186197118-G-A
MyVariant Identifiers: chr4:g.187118272G>A (hg19) chr4:g.186197118G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197118G>A , CM000666.2:g.186197118G>A GRCh38
NC_000004.11:g.187118272G>A , CM000666.1:g.187118272G>A GRCh37
NC_000004.10:g.187355266G>A NCBI36
NG_007965.1:g.10599G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.592G>A MANE Select ENSP00000368079.4:p.Asp198Asn
ENST00000378802.4:c.592G>A ENSP00000368079.4:p.Asp198Asn
ENST00000507209.5:n.1031G>A
NM_207352.3:c.592G>A NP_997235.3:p.Asp198Asn
XM_005262935.2:c.592G>A XP_005262992.1:p.Asp198Asn
XM_006714184.2:c.196G>A XP_006714247.1:p.Asp66Asn
XM_005262935.4:c.592G>A XP_005262992.1:p.Asp198Asn
XM_017008037.1:c.196G>A XP_016863526.1:p.Asp66Asn
NM_207352.4:c.592G>A MANE Select NP_997235.3:p.Asp198Asn
Search 100 bp 5'
Search 100 bp 3'