Canonical Allele Identifier: CA2672897393

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197336-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197336G>T , CM000666.2:g.186197336G>T	GRCh38
NC_000004.11:g.187118490G>T , CM000666.1:g.187118490G>T	GRCh37
NC_000004.10:g.187355484G>T	NCBI36
NG_007965.1:g.10817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.605-197G>T MANE Select	ENSP00000368079.4:n.605-197G>T
ENST00000378802.4:c.605-197G>T	ENSP00000368079.4:n.605-197G>T
ENST00000507209.5:n.1249G>T
NM_207352.3:c.605-197G>T	NP_997235.3:n.605-197G>T
XM_005262935.2:c.605-197G>T	XP_005262992.1:n.605-197G>T
XM_006714184.2:c.209-197G>T	XP_006714247.1:n.209-197G>T
XM_005262935.4:c.605-197G>T	XP_005262992.1:n.605-197G>T
XM_017008037.1:c.209-197G>T	XP_016863526.1:n.209-197G>T
NM_207352.4:c.605-197G>T MANE Select	NP_997235.3:n.605-197G>T