Canonical Allele Identifier: CA358947613
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186197103-A-G
MyVariant Identifiers: chr4:g.187118257A>G (hg19) chr4:g.186197103A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197103A>G , CM000666.2:g.186197103A>G GRCh38
NC_000004.11:g.187118257A>G , CM000666.1:g.187118257A>G GRCh37
NC_000004.10:g.187355251A>G NCBI36
NG_007965.1:g.10584A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.577A>G MANE Select ENSP00000368079.4:p.Thr193Ala
ENST00000378802.4:c.577A>G ENSP00000368079.4:p.Thr193Ala
ENST00000507209.5:n.1016A>G
NM_207352.3:c.577A>G NP_997235.3:p.Thr193Ala
XM_005262935.2:c.577A>G XP_005262992.1:p.Thr193Ala
XM_006714184.2:c.181A>G XP_006714247.1:p.Thr61Ala
XM_005262935.4:c.577A>G XP_005262992.1:p.Thr193Ala
XM_017008037.1:c.181A>G XP_016863526.1:p.Thr61Ala
NM_207352.4:c.577A>G MANE Select NP_997235.3:p.Thr193Ala
Search 100 bp 5'
Search 100 bp 3'