Canonical Allele Identifier: CA1315935860

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190205112T= , CM000664.2:g.190205112T=	GRCh38
NC_000002.11:g.191069838T= , CM000664.1:g.191069838T=	GRCh37
NC_000002.10:g.190778083T=	NCBI36
NG_017062.1:g.119934A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359678.10:c.*5A= MANE Select	ENSP00000352706.5:n.*5A=
ENST00000359678.9:c.*5A=	ENSP00000352706.5:n.*5A=
ENST00000392332.7:c.*115A=	ENSP00000376144.3:n.*115A=
ENST00000399855.2:c.121A=
ENST00000410045.5:c.*5A=	ENSP00000386274.1:n.*5A=
ENST00000486981.1:n.401A=
ENST00000622246.4:c.*5A=	ENSP00000481055.1:n.*5A=
NM_014362.3:c.*5A=	NP_055177.2:n.*5A=
NM_198047.2:c.*115A=	NP_932164.1:n.*115A=
XM_011510953.1:c.*5A=	XP_011509255.1:n.*5A=
XM_011510954.1:c.*5A=	XP_011509256.1:n.*5A=
XR_922903.1:n.1376A=
XM_011510953.2:c.*5A=	XP_011509255.1:n.*5A=
XR_922903.2:n.1195A=
NM_014362.4:c.*5A= MANE Select	NP_055177.2:n.*5A=
NM_198047.3:c.*115A=	NP_932164.1:n.*115A=