Canonical Allele Identifier: CA358946740
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186192019-A-G
MyVariant Identifiers: chr4:g.187113173A>G (hg19) chr4:g.186192019A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186192019A>G , CM000666.2:g.186192019A>G GRCh38
NC_000004.11:g.187113173A>G , CM000666.1:g.187113173A>G GRCh37
NC_000004.10:g.187350167A>G NCBI36
NG_007965.1:g.5500A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.196A>G MANE Select ENSP00000368079.4:p.Met66Val
ENST00000378802.4:c.196A>G ENSP00000368079.4:p.Met66Val
NM_207352.3:c.196A>G NP_997235.3:p.Met66Val
XM_005262935.2:c.196A>G XP_005262992.1:p.Met66Val
XM_005262935.4:c.196A>G XP_005262992.1:p.Met66Val
XM_017008037.1:c.-115A>G XP_016863526.1:n.-115A>G
NM_207352.4:c.196A>G MANE Select NP_997235.3:p.Met66Val
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