Canonical Allele Identifier: CA349894318

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190213017C>A , CM000664.2:g.190213017C>A	GRCh38
NC_000002.11:g.191077743C>A , CM000664.1:g.191077743C>A	GRCh37
NC_000002.10:g.190785988C>A	NCBI36
NG_017062.1:g.112029G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014362.4:c.950G>T MANE Select	NP_055177.2:p.Gly317Val
ENST00000359678.10:c.950G>T MANE Select	ENSP00000352706.5:p.Gly317Val
NM_014362.3:c.950G>T	NP_055177.2:p.Gly317Val
NM_198047.2:c.950G>T	NP_932164.1:p.Gly317Val
NM_198047.3:c.950G>T	NP_932164.1:p.Gly317Val
ENST00000359678.9:c.950G>T	ENSP00000352706.5:p.Gly317Val
ENST00000392332.7:c.950G>T	ENSP00000376144.3:p.Gly317Val
ENST00000409820.2:c.290G>T	ENSP00000387098.2:p.Gly97Val
ENST00000410045.5:c.281G>T	ENSP00000386274.1:p.Gly94Val
ENST00000416732.5:c.203G>T	ENSP00000399263.1:p.Gly68Val
ENST00000486981.1:n.219G>T
ENST00000489147.1:n.3093G>T
ENST00000622246.4:c.932G>T	ENSP00000481055.1:p.Gly311Val
XM_011510953.1:c.950G>T	XP_011509255.1:p.Gly317Val
XM_011510953.2:c.950G>T	XP_011509255.1:p.Gly317Val
XM_011510954.1:c.452G>T	XP_011509256.1:p.Gly151Val
XR_922903.1:n.1194G>T
XR_922903.2:n.1013G>T