Canonical Allele Identifier: CA1315956034

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190248198T= , CM000664.2:g.190248198T=	GRCh38
NC_000002.11:g.191112924T= , CM000664.1:g.191112924T=	GRCh37
NC_000002.10:g.190821169T=	NCBI36
NG_017062.1:g.76848A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000359678.10:c.750+1442A= MANE Select	ENSP00000352706.5:n.750+1442A=
ENST00000359678.9:c.750+1442A=	ENSP00000352706.5:n.750+1442A=
ENST00000392332.7:c.750+1442A=	ENSP00000376144.3:n.750+1442A=
ENST00000392333.7:c.367+1442A=
ENST00000409820.2:c.90+1442A=	ENSP00000387098.2:n.90+1442A=
ENST00000410045.5:c.81+1442A=	ENSP00000386274.1:n.81+1442A=
ENST00000485992.1:n.371+1442A=
ENST00000622246.4:c.732+1442A=	ENSP00000481055.1:n.732+1442A=
NM_014362.3:c.750+1442A=	NP_055177.2:n.750+1442A=
NM_198047.2:c.750+1442A=	NP_932164.1:n.750+1442A=
XM_011510953.1:c.750+1442A=	XP_011509255.1:n.750+1442A=
XM_011510954.1:c.252+1442A=	XP_011509256.1:n.252+1442A=
XR_922903.1:n.994+1442A=
XM_011510953.2:c.750+1442A=	XP_011509255.1:n.750+1442A=
XR_922903.2:n.813+1442A=
NM_014362.4:c.750+1442A= MANE Select	NP_055177.2:n.750+1442A=
NM_198047.3:c.750+1442A=	NP_932164.1:n.750+1442A=