Canonical Allele Identifier: CA442638745
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187115754A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194600A>T , CM000666.2:g.186194600A>T GRCh38
NC_000004.11:g.187115754A>T , CM000666.1:g.187115754A>T GRCh37
NC_000004.10:g.187352748A>T NCBI36
NG_007965.1:g.8081A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.315A>T MANE Select ENSP00000368079.4:p.Ala105=
ENST00000378802.4:c.315A>T ENSP00000368079.4:p.Ala105=
NM_207352.3:c.315A>T NP_997235.3:p.Ala105=
XM_005262935.2:c.315A>T XP_005262992.1:p.Ala105=
XM_006714184.2:c.5A>T XP_006714247.1:p.Gln2Leu
XM_005262935.4:c.315A>T XP_005262992.1:p.Ala105=
XM_017008037.1:c.5A>T XP_016863526.1:p.Gln2Leu
NM_207352.4:c.315A>T MANE Select NP_997235.3:p.Ala105=