Canonical Allele Identifier: CA349894321

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190213018C>G , CM000664.2:g.190213018C>G	GRCh38
NC_000002.11:g.191077744C>G , CM000664.1:g.191077744C>G	GRCh37
NC_000002.10:g.190785989C>G	NCBI36
NG_017062.1:g.112028G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014362.4:c.949G>C MANE Select	NP_055177.2:p.Gly317Arg
ENST00000359678.10:c.949G>C MANE Select	ENSP00000352706.5:p.Gly317Arg
NM_014362.3:c.949G>C	NP_055177.2:p.Gly317Arg
NM_198047.2:c.949G>C	NP_932164.1:p.Gly317Arg
NM_198047.3:c.949G>C	NP_932164.1:p.Gly317Arg
ENST00000359678.9:c.949G>C	ENSP00000352706.5:p.Gly317Arg
ENST00000392332.7:c.949G>C	ENSP00000376144.3:p.Gly317Arg
ENST00000409820.2:c.289G>C	ENSP00000387098.2:p.Gly97Arg
ENST00000410045.5:c.280G>C	ENSP00000386274.1:p.Gly94Arg
ENST00000416732.5:c.202G>C	ENSP00000399263.1:p.Gly68Arg
ENST00000486981.1:n.218G>C
ENST00000489147.1:n.3092G>C
ENST00000622246.4:c.931G>C	ENSP00000481055.1:p.Gly311Arg
XM_011510953.1:c.949G>C	XP_011509255.1:p.Gly317Arg
XM_011510953.2:c.949G>C	XP_011509255.1:p.Gly317Arg
XM_011510954.1:c.451G>C	XP_011509256.1:p.Gly151Arg
XR_922903.1:n.1193G>C
XR_922903.2:n.1012G>C