Canonical Allele Identifier: CA358946505
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1299718485
gnomAD v2: 4-187113054-G-T
gnomAD v4: 4-186191900-G-T
MyVariant Identifiers: chr4:g.187113054G>T (hg19) chr4:g.186191900G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191900G>T , CM000666.2:g.186191900G>T GRCh38
NC_000004.11:g.187113054G>T , CM000666.1:g.187113054G>T GRCh37
NC_000004.10:g.187350048G>T NCBI36
NG_007965.1:g.5381G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.77G>T MANE Select ENSP00000368079.4:p.Gly26Val
ENST00000378802.4:c.77G>T ENSP00000368079.4:p.Gly26Val
NM_207352.3:c.77G>T NP_997235.3:p.Gly26Val
XM_005262935.2:c.77G>T XP_005262992.1:p.Gly26Val
XM_005262935.4:c.77G>T XP_005262992.1:p.Gly26Val
XM_017008037.1:c.-234G>T XP_016863526.1:n.-234G>T
NM_207352.4:c.77G>T MANE Select NP_997235.3:p.Gly26Val
Search 100 bp 5'
Search 100 bp 3'