Canonical Allele Identifier: CA1315935831

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190205039A= , CM000664.2:g.190205039A=	GRCh38
NC_000002.11:g.191069765A= , CM000664.1:g.191069765A=	GRCh37
NC_000002.10:g.190778010A=	NCBI36
NG_017062.1:g.120007T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359678.10:c.*78T= MANE Select	ENSP00000352706.5:n.*78T=
ENST00000359678.9:c.*78T=	ENSP00000352706.5:n.*78T=
ENST00000392332.7:c.*188T=	ENSP00000376144.3:n.*188T=
ENST00000399855.2:c.133+61T=
ENST00000410045.5:c.*78T=	ENSP00000386274.1:n.*78T=
ENST00000486981.1:n.413+61T=
ENST00000622246.4:c.*78T=	ENSP00000481055.1:n.*78T=
NM_014362.3:c.*78T=	NP_055177.2:n.*78T=
NM_198047.2:c.*188T=	NP_932164.1:n.*188T=
XM_011510953.1:c.*17+61T=	XP_011509255.1:n.*17+61T=
XM_011510954.1:c.*78T=	XP_011509256.1:n.*78T=
XR_922903.1:n.1388+61T=
XM_011510953.2:c.*17+61T=	XP_011509255.1:n.*17+61T=
XR_922903.2:n.1207+61T=
NM_014362.4:c.*78T= MANE Select	NP_055177.2:n.*78T=
NM_198047.3:c.*188T=	NP_932164.1:n.*188T=