Canonical Allele Identifier: CA1315935866
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190205139C= , CM000664.2:g.190205139C= GRCh38
NC_000002.11:g.191069865C= , CM000664.1:g.191069865C= GRCh37
NC_000002.10:g.190778110C= NCBI36
NG_017062.1:g.119907G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359678.10:c.1139G= MANE Select ENSP00000352706.5:p.Gly380=
ENST00000359678.9:c.1139G= ENSP00000352706.5:p.Gly380=
ENST00000392332.7:c.*88G= ENSP00000376144.3:n.*88G=
ENST00000399855.2:c.94G=
ENST00000410045.5:c.470G= ENSP00000386274.1:p.Gly157=
ENST00000486981.1:n.374G=
ENST00000622246.4:c.1121G= ENSP00000481055.1:p.Gly374=
NM_014362.3:c.1139G= NP_055177.2:p.Gly380=
NM_198047.2:c.*88G= NP_932164.1:n.*88G=
XM_011510953.1:c.1139G= XP_011509255.1:p.Gly380=
XM_011510954.1:c.641G= XP_011509256.1:p.Gly214=
XR_922903.1:n.1349G=
XM_011510953.2:c.1139G= XP_011509255.1:p.Gly380=
XR_922903.2:n.1168G=
NM_014362.4:c.1139G= MANE Select NP_055177.2:p.Gly380=
NM_198047.3:c.*88G= NP_932164.1:n.*88G=