Canonical Allele Identifier: CA358947255

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187118101A>G (hg19) ; chr4:g.186196947A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186196947A>G , CM000666.2:g.186196947A>G	GRCh38
NC_000004.11:g.187118101A>G , CM000666.1:g.187118101A>G	GRCh37
NC_000004.10:g.187355095A>G	NCBI36
NG_007965.1:g.10428A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.421A>G MANE Select	ENSP00000368079.4:p.Asn141Asp
ENST00000378802.4:c.421A>G	ENSP00000368079.4:p.Asn141Asp
ENST00000507209.5:n.860A>G
NM_207352.3:c.421A>G	NP_997235.3:p.Asn141Asp
XM_005262935.2:c.421A>G	XP_005262992.1:p.Asn141Asp
XM_006714184.2:c.25A>G	XP_006714247.1:p.Asn9Asp
XM_005262935.4:c.421A>G	XP_005262992.1:p.Asn141Asp
XM_017008037.1:c.25A>G	XP_016863526.1:p.Asn9Asp
NM_207352.4:c.421A>G MANE Select	NP_997235.3:p.Asn141Asp