Canonical Allele Identifier: CA1315935895

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190205214T= , CM000664.2:g.190205214T=	GRCh38
NC_000002.11:g.191069940T= , CM000664.1:g.191069940T=	GRCh37
NC_000002.10:g.190778185T=	NCBI36
NG_017062.1:g.119832A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359678.10:c.1064A= MANE Select	ENSP00000352706.5:p.Gln355=
ENST00000359678.9:c.1064A=	ENSP00000352706.5:p.Gln355=
ENST00000392332.7:c.*13A=	ENSP00000376144.3:n.*13A=
ENST00000399855.2:c.19A=
ENST00000410045.5:c.395A=	ENSP00000386274.1:p.Gln132=
ENST00000486981.1:n.299A=
ENST00000622246.4:c.1046A=	ENSP00000481055.1:p.Gln349=
NM_014362.3:c.1064A=	NP_055177.2:p.Gln355=
NM_198047.2:c.*13A=	NP_932164.1:n.*13A=
XM_011510953.1:c.1064A=	XP_011509255.1:p.Gln355=
XM_011510954.1:c.566A=	XP_011509256.1:p.Gln189=
XR_922903.1:n.1274A=
XM_011510953.2:c.1064A=	XP_011509255.1:p.Gln355=
XR_922903.2:n.1093A=
NM_014362.4:c.1064A= MANE Select	NP_055177.2:p.Gln355=
NM_198047.3:c.*13A=	NP_932164.1:n.*13A=