Canonical Allele Identifier: CA1315935824

Gene: HIBCH

Linked Data

• dbSNP Id: rs554673601

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190205027G>T , CM000664.2:g.190205027G>T	GRCh38
NC_000002.11:g.191069753G>T , CM000664.1:g.191069753G>T	GRCh37
NC_000002.10:g.190777998G>T	NCBI36
NG_017062.1:g.120019C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359678.10:c.*90C>A MANE Select	ENSP00000352706.5:n.*90C>A
ENST00000359678.9:c.*90C>A	ENSP00000352706.5:n.*90C>A
ENST00000392332.7:c.*200C>A	ENSP00000376144.3:n.*200C>A
ENST00000399855.2:c.133+73C>A
ENST00000410045.5:c.*90C>A	ENSP00000386274.1:n.*90C>A
ENST00000486981.1:n.413+73C>A
ENST00000622246.4:c.*90C>A	ENSP00000481055.1:n.*90C>A
NM_014362.3:c.*90C>A	NP_055177.2:n.*90C>A
NM_198047.2:c.*200C>A	NP_932164.1:n.*200C>A
XM_011510953.1:c.*17+73C>A	XP_011509255.1:n.*17+73C>A
XM_011510954.1:c.*90C>A	XP_011509256.1:n.*90C>A
XR_922903.1:n.1388+73C>A
XM_011510953.2:c.*17+73C>A	XP_011509255.1:n.*17+73C>A
XR_922903.2:n.1207+73C>A
NM_014362.4:c.*90C>A MANE Select	NP_055177.2:n.*90C>A
NM_198047.3:c.*200C>A	NP_932164.1:n.*200C>A