Canonical Allele Identifier: CA349894346

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190213029T>C , CM000664.2:g.190213029T>C	GRCh38
NC_000002.11:g.191077755T>C , CM000664.1:g.191077755T>C	GRCh37
NC_000002.10:g.190786000T>C	NCBI36
NG_017062.1:g.112017A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014362.4:c.938A>G MANE Select	NP_055177.2:p.Gln313Arg
ENST00000359678.10:c.938A>G MANE Select	ENSP00000352706.5:p.Gln313Arg
NM_014362.3:c.938A>G	NP_055177.2:p.Gln313Arg
NM_198047.2:c.938A>G	NP_932164.1:p.Gln313Arg
NM_198047.3:c.938A>G	NP_932164.1:p.Gln313Arg
ENST00000359678.9:c.938A>G	ENSP00000352706.5:p.Gln313Arg
ENST00000392332.7:c.938A>G	ENSP00000376144.3:p.Gln313Arg
ENST00000409820.2:c.278A>G	ENSP00000387098.2:p.Gln93Arg
ENST00000410045.5:c.269A>G	ENSP00000386274.1:p.Gln90Arg
ENST00000416732.5:c.191A>G	ENSP00000399263.1:p.Gln64Arg
ENST00000486981.1:n.207A>G
ENST00000489147.1:n.3081A>G
ENST00000622246.4:c.920A>G	ENSP00000481055.1:p.Gln307Arg
XM_011510953.1:c.938A>G	XP_011509255.1:p.Gln313Arg
XM_011510953.2:c.938A>G	XP_011509255.1:p.Gln313Arg
XM_011510954.1:c.440A>G	XP_011509256.1:p.Gln147Arg
XR_922903.1:n.1182A>G
XR_922903.2:n.1001A>G