Canonical Allele Identifier: CA349894348

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190213030G>C , CM000664.2:g.190213030G>C	GRCh38
NC_000002.11:g.191077756G>C , CM000664.1:g.191077756G>C	GRCh37
NC_000002.10:g.190786001G>C	NCBI36
NG_017062.1:g.112016C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014362.4:c.937C>G MANE Select	NP_055177.2:p.Gln313Glu
ENST00000359678.10:c.937C>G MANE Select	ENSP00000352706.5:p.Gln313Glu
NM_014362.3:c.937C>G	NP_055177.2:p.Gln313Glu
NM_198047.2:c.937C>G	NP_932164.1:p.Gln313Glu
NM_198047.3:c.937C>G	NP_932164.1:p.Gln313Glu
ENST00000359678.9:c.937C>G	ENSP00000352706.5:p.Gln313Glu
ENST00000392332.7:c.937C>G	ENSP00000376144.3:p.Gln313Glu
ENST00000409820.2:c.277C>G	ENSP00000387098.2:p.Gln93Glu
ENST00000410045.5:c.268C>G	ENSP00000386274.1:p.Gln90Glu
ENST00000416732.5:c.190C>G	ENSP00000399263.1:p.Gln64Glu
ENST00000486981.1:n.206C>G
ENST00000489147.1:n.3080C>G
ENST00000622246.4:c.919C>G	ENSP00000481055.1:p.Gln307Glu
XM_011510953.1:c.937C>G	XP_011509255.1:p.Gln313Glu
XM_011510953.2:c.937C>G	XP_011509255.1:p.Gln313Glu
XM_011510954.1:c.439C>G	XP_011509256.1:p.Gln147Glu
XR_922903.1:n.1181C>G
XR_922903.2:n.1000C>G