Canonical Allele Identifier: CA2753610228

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190248203G>A , CM000664.2:g.190248203G>A	GRCh38
NC_000002.11:g.191112929G>A , CM000664.1:g.191112929G>A	GRCh37
NC_000002.10:g.190821174G>A	NCBI36
NG_017062.1:g.76843C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359678.10:c.750+1437C>T MANE Select	ENSP00000352706.5:n.750+1437C>T
ENST00000359678.9:c.750+1437C>T	ENSP00000352706.5:n.750+1437C>T
ENST00000392332.7:c.750+1437C>T	ENSP00000376144.3:n.750+1437C>T
ENST00000392333.7:c.367+1437C>T
ENST00000409820.2:c.90+1437C>T	ENSP00000387098.2:n.90+1437C>T
ENST00000410045.5:c.81+1437C>T	ENSP00000386274.1:n.81+1437C>T
ENST00000485992.1:n.371+1437C>T
ENST00000622246.4:c.732+1437C>T	ENSP00000481055.1:n.732+1437C>T
NM_014362.3:c.750+1437C>T	NP_055177.2:n.750+1437C>T
NM_198047.2:c.750+1437C>T	NP_932164.1:n.750+1437C>T
XM_011510953.1:c.750+1437C>T	XP_011509255.1:n.750+1437C>T
XM_011510954.1:c.252+1437C>T	XP_011509256.1:n.252+1437C>T
XR_922903.1:n.994+1437C>T
XM_011510953.2:c.750+1437C>T	XP_011509255.1:n.750+1437C>T
XR_922903.2:n.813+1437C>T
NM_014362.4:c.750+1437C>T MANE Select	NP_055177.2:n.750+1437C>T
NM_198047.3:c.750+1437C>T	NP_932164.1:n.750+1437C>T