Canonical Allele Identifier: CA2258514326
Gene: HNF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.37701306G= , CM000679.2:g.37701306G= GRCh38
NC_000017.10:g.36061311G= , CM000679.1:g.36061311G= GRCh37
NC_000017.9:g.33135424G= NCBI36
NG_013019.2:g.48801C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617811.5:c.1340-129C= MANE Select ENSP00000480291.1:n.1340-129C=
ENST00000613727.4:c.1261+3611C= ENSP00000477524.1:n.1261+3611C=
ENST00000614313.4:c.1340-129C= ENSP00000482529.1:n.1340-129C=
ENST00000617272.4:c.*63-129C= ENSP00000478682.1:n.*63-129C=
ENST00000617811.4:c.1340-129C= ENSP00000480291.1:n.1340-129C=
ENST00000621123.4:c.1262-129C= ENSP00000482711.1:n.1262-129C=
NM_000458.3:c.1340-129C= NP_000449.1:n.1340-129C=
NM_001165923.3:c.1262-129C= NP_001159395.1:n.1262-129C=
NM_001304286.1:c.1261+3611C= NP_001291215.1:n.1261+3611C=
XM_011525160.1:c.1340-129C= XP_011523462.1:n.1340-129C=
XM_011525161.1:c.1340-2112C= XP_011523463.1:n.1340-2112C=
XM_011525164.1:c.1262-129C= XP_011523466.1:n.1262-129C=
NM_000458.4:c.1340-129C= MANE Select NP_000449.1:n.1340-129C=
NM_001165923.4:c.1262-129C= NP_001159395.1:n.1262-129C=
NM_001304286.2:c.1261+3611C= NP_001291215.1:n.1261+3611C=