Canonical Allele Identifier: CA358946511
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187113057C>T (hg19) chr4:g.186191903C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191903C>T , CM000666.2:g.186191903C>T GRCh38
NC_000004.11:g.187113057C>T , CM000666.1:g.187113057C>T GRCh37
NC_000004.10:g.187350051C>T NCBI36
NG_007965.1:g.5384C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.80C>T MANE Select ENSP00000368079.4:p.Ala27Val
ENST00000378802.4:c.80C>T ENSP00000368079.4:p.Ala27Val
NM_207352.3:c.80C>T NP_997235.3:p.Ala27Val
XM_005262935.2:c.80C>T XP_005262992.1:p.Ala27Val
XM_005262935.4:c.80C>T XP_005262992.1:p.Ala27Val
XM_017008037.1:c.-231C>T XP_016863526.1:n.-231C>T
NM_207352.4:c.80C>T MANE Select NP_997235.3:p.Ala27Val
Search 100 bp 5'
Search 100 bp 3'