Canonical Allele Identifier: CA2576244014

Gene: HNF1B

Linked Data

• ClinVar Variation Id: 3053481
• ClinVar RCV Id: RCV003964046
• gnomAD v4: 17-37731589-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37731589G>A , CM000679.2:g.37731589G>A	GRCh38
NC_000017.10:g.36091580G>A , CM000679.1:g.36091580G>A	GRCh37
NC_000017.9:g.33165693G>A	NCBI36
NG_013019.2:g.18518C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.1045+6C>T MANE Select	ENSP00000480291.1:n.1045+6C>T
ENST00000613727.4:c.967+6C>T	ENSP00000477524.1:n.967+6C>T
ENST00000614313.4:c.1045+6C>T	ENSP00000482529.1:n.1045+6C>T
ENST00000617272.4:c.1045+6C>T	ENSP00000478682.1:n.1045+6C>T
ENST00000617811.4:c.1045+6C>T	ENSP00000480291.1:n.1045+6C>T
ENST00000618894.1:n.503C>T
ENST00000621123.4:c.967+6C>T	ENSP00000482711.1:n.967+6C>T
NM_000458.3:c.1045+6C>T	NP_000449.1:n.1045+6C>T
NM_001165923.3:c.967+6C>T	NP_001159395.1:n.967+6C>T
NM_001304286.1:c.967+6C>T	NP_001291215.1:n.967+6C>T
XM_011525160.1:c.1045+6C>T	XP_011523462.1:n.1045+6C>T
XM_011525161.1:c.1045+6C>T	XP_011523463.1:n.1045+6C>T
XM_011525162.1:c.1045+6C>T	XP_011523464.1:n.1045+6C>T
XM_011525163.1:c.1045+6C>T	XP_011523465.1:n.1045+6C>T
XM_011525164.1:c.967+6C>T	XP_011523466.1:n.967+6C>T
XM_011525162.2:c.1045+6C>T	XP_011523464.1:n.1045+6C>T
XM_011525163.2:c.1045+6C>T	XP_011523465.1:n.1045+6C>T
NM_000458.4:c.1045+6C>T MANE Select	NP_000449.1:n.1045+6C>T
NM_001165923.4:c.967+6C>T	NP_001159395.1:n.967+6C>T
NM_001304286.2:c.967+6C>T	NP_001291215.1:n.967+6C>T