Canonical Allele Identifier: CA499602785

Gene: HNF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37733663G>T , CM000679.2:g.37733663G>T	GRCh38
NC_000017.10:g.36093656G>T , CM000679.1:g.36093656G>T	GRCh37
NC_000017.9:g.33167769G>T	NCBI36
NG_013019.2:g.16444C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.703C>A MANE Select	ENSP00000480291.1:p.Arg235=
ENST00000613727.4:c.625C>A	ENSP00000477524.1:p.Arg209=
ENST00000614313.4:c.703C>A	ENSP00000482529.1:p.Arg235=
ENST00000617272.4:c.703C>A	ENSP00000478682.1:p.Arg235=
ENST00000617811.4:c.703C>A	ENSP00000480291.1:p.Arg235=
ENST00000618894.1:n.155C>A
ENST00000620125.1:c.625C>A	ENSP00000481245.1:p.Arg209=
ENST00000621123.4:c.625C>A	ENSP00000482711.1:p.Arg209=
NM_000458.3:c.703C>A	NP_000449.1:p.Arg235=
NM_001165923.3:c.625C>A	NP_001159395.1:p.Arg209=
NM_001304286.1:c.625C>A	NP_001291215.1:p.Arg209=
XM_011525160.1:c.703C>A	XP_011523462.1:p.Arg235=
XM_011525161.1:c.703C>A	XP_011523463.1:p.Arg235=
XM_011525162.1:c.703C>A	XP_011523464.1:p.Arg235=
XM_011525163.1:c.703C>A	XP_011523465.1:p.Arg235=
XM_011525164.1:c.625C>A	XP_011523466.1:p.Arg209=
XM_011525162.2:c.703C>A	XP_011523464.1:p.Arg235=
XM_011525163.2:c.703C>A	XP_011523465.1:p.Arg235=
NM_000458.4:c.703C>A MANE Select	NP_000449.1:p.Arg235=
NM_001165923.4:c.625C>A	NP_001159395.1:p.Arg209=
NM_001304286.2:c.625C>A	NP_001291215.1:p.Arg209=