Canonical Allele Identifier: CA2672895367

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186194672-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194672C>T , CM000666.2:g.186194672C>T	GRCh38
NC_000004.11:g.187115826C>T , CM000666.1:g.187115826C>T	GRCh37
NC_000004.10:g.187352820C>T	NCBI36
NG_007965.1:g.8153C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.327+60C>T MANE Select	ENSP00000368079.4:n.327+60C>T
ENST00000378802.4:c.327+60C>T	ENSP00000368079.4:n.327+60C>T
NM_207352.3:c.327+60C>T	NP_997235.3:n.327+60C>T
XM_005262935.2:c.327+60C>T	XP_005262992.1:n.327+60C>T
XM_006714184.2:c.17+60C>T	XP_006714247.1:n.17+60C>T
XM_005262935.4:c.327+60C>T	XP_005262992.1:n.327+60C>T
XM_017008037.1:c.17+60C>T	XP_016863526.1:n.17+60C>T
NM_207352.4:c.327+60C>T MANE Select	NP_997235.3:n.327+60C>T