Canonical Allele Identifier: CA1140322811

Gene: CYP4B1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46819251T= , CM000663.2:g.46819251T=	GRCh38
NC_000001.10:g.47284923T= , CM000663.1:g.47284923T=	GRCh37
NC_000001.9:g.47057510T=	NCBI36
NG_007939.1:g.25254T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371923.9:c.*437T= MANE Select	ENSP00000360991.4:n.*437T=
ENST00000271153.8:c.*437T=	ENSP00000271153.4:n.*437T=
ENST00000371923.8:c.*437T=	ENSP00000360991.4:n.*437T=
ENST00000464439.6:c.*925T=	ENSP00000433068.1:n.*925T=
NM_000779.3:c.*437T=	NP_000770.2:n.*437T=
NM_001099772.1:c.*437T=	NP_001093242.1:n.*437T=
XM_011540831.1:c.*437T=	XP_011539133.1:n.*437T=
XM_011540833.1:c.*437T=	XP_011539135.1:n.*437T=
XM_011540834.1:c.*437T=	XP_011539136.1:n.*437T=
NM_001319161.1:c.*437T=	NP_001306090.1:n.*437T=
NM_001319162.1:c.*437T=	NP_001306091.1:n.*437T=
NM_001319163.1:c.*437T=	NP_001306092.1:n.*437T=
NR_135003.1:n.1987T=
XM_017000466.1:c.*437T=	XP_016855955.1:n.*437T=
NM_000779.4:c.*437T=	NP_000770.2:n.*437T=
NM_001099772.2:c.*437T= MANE Select	NP_001093242.1:n.*437T=
NM_001319161.2:c.*437T=	NP_001306090.1:n.*437T=
NM_001319162.2:c.*437T=	NP_001306091.1:n.*437T=
NM_001319163.2:c.*437T=	NP_001306092.1:n.*437T=
NR_135003.2:n.1939T=