Canonical Allele Identifier: CA112127198

Gene: CYP4V2

Linked Data

• dbSNP Id: rs919982174
• gnomAD v3: 4-186200634-G-C
• gnomAD v4: 4-186200634-G-C
• MyVariant Identifiers: chr4:g.187121788G>C (hg19) ; chr4:g.186200634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200634G>C , CM000666.2:g.186200634G>C	GRCh38
NC_000004.11:g.187121788G>C , CM000666.1:g.187121788G>C	GRCh37
NC_000004.10:g.187358782G>C	NCBI36
NG_007965.1:g.14115G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-523G>C MANE Select	ENSP00000368079.4:n.802-523G>C
ENST00000378802.4:c.802-523G>C	ENSP00000368079.4:n.802-523G>C
ENST00000507209.5:n.1643-523G>C
NM_207352.3:c.802-523G>C	NP_997235.3:n.802-523G>C
XM_005262935.2:c.802-523G>C	XP_005262992.1:n.802-523G>C
XM_006714184.2:c.406-523G>C	XP_006714247.1:n.406-523G>C
XM_005262935.4:c.802-523G>C	XP_005262992.1:n.802-523G>C
XM_017008037.1:c.406-523G>C	XP_016863526.1:n.406-523G>C
NM_207352.4:c.802-523G>C MANE Select	NP_997235.3:n.802-523G>C