Canonical Allele Identifier: CA2027427
Community Standard Title: NM_014362.4(HIBCH):c.937C>T (p.Gln313Ter)
Gene: HIBCH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.937C>T MANE Select NP_055177.2:p.Gln313Ter
ENST00000359678.10:c.937C>T MANE Select ENSP00000352706.5:p.Gln313Ter
NM_014362.3:c.937C>T NP_055177.2:p.Gln313Ter
NM_198047.2:c.937C>T NP_932164.1:p.Gln313Ter
NM_198047.3:c.937C>T NP_932164.1:p.Gln313Ter
ENST00000359678.9:c.937C>T ENSP00000352706.5:p.Gln313Ter
ENST00000392332.7:c.937C>T ENSP00000376144.3:p.Gln313Ter
ENST00000409820.2:c.277C>T ENSP00000387098.2:p.Gln93Ter
ENST00000410045.5:c.268C>T ENSP00000386274.1:p.Gln90Ter
ENST00000416732.5:c.190C>T ENSP00000399263.1:p.Gln64Ter
ENST00000486981.1:n.206C>T
ENST00000489147.1:n.3080C>T
ENST00000622246.4:c.919C>T ENSP00000481055.1:p.Gln307Ter
XM_011510953.1:c.937C>T XP_011509255.1:p.Gln313Ter
XM_011510953.2:c.937C>T XP_011509255.1:p.Gln313Ter
XM_011510954.1:c.439C>T XP_011509256.1:p.Gln147Ter
XR_922903.1:n.1181C>T
XR_922903.2:n.1000C>T