Canonical Allele Identifier: CA2497420800

Gene: HNF1B

Linked Data

• dbSNP Id: rs2034134199

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37745026del , CM000679.2:g.37745026del	GRCh38
NC_000017.10:g.36105017del , CM000679.1:g.36105017del	GRCh37
NC_000017.9:g.33179130del	NCBI36
NG_013019.2:g.5083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.-140del MANE Select	ENSP00000480291.1:n.-140del
ENST00000617811.4:c.-140del	ENSP00000480291.1:n.-140del
ENST00000620125.1:c.-140del	ENSP00000481245.1:n.-140del
ENST00000621123.4:c.-140del	ENSP00000482711.1:n.-140del
NM_000458.3:c.-140del	NP_000449.1:n.-140del
NM_001165923.3:c.-140del	NP_001159395.1:n.-140del
NM_001304286.1:c.-140del	NP_001291215.1:n.-140del
XM_011525160.1:c.-140del	XP_011523462.1:n.-140del
XM_011525161.1:c.-140del	XP_011523463.1:n.-140del
XM_011525162.1:c.-140del	XP_011523464.1:n.-140del
XM_011525163.1:c.-140del	XP_011523465.1:n.-140del
XM_011525164.1:c.-140del	XP_011523466.1:n.-140del
XM_011525162.2:c.-140del	XP_011523464.1:n.-140del
XM_011525163.2:c.-140del	XP_011523465.1:n.-140del
NM_000458.4:c.-140del MANE Select	NP_000449.1:n.-140del
NM_001165923.4:c.-140del	NP_001159395.1:n.-140del
NM_001304286.2:c.-140del	NP_001291215.1:n.-140del