Canonical Allele Identifier: CA2637449758

Gene: HNF1B

Linked Data

• gnomAD v4: 17-37745037-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37745037C>A , CM000679.2:g.37745037C>A	GRCh38
NC_000017.10:g.36105028C>A , CM000679.1:g.36105028C>A	GRCh37
NC_000017.9:g.33179141C>A	NCBI36
NG_013019.2:g.5070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617811.5:c.-153G>T MANE Select	ENSP00000480291.1:n.-153G>T
ENST00000617811.4:c.-153G>T	ENSP00000480291.1:n.-153G>T
ENST00000620125.1:c.-153G>T	ENSP00000481245.1:n.-153G>T
ENST00000621123.4:c.-153G>T	ENSP00000482711.1:n.-153G>T
NM_000458.3:c.-153G>T	NP_000449.1:n.-153G>T
NM_001165923.3:c.-153G>T	NP_001159395.1:n.-153G>T
NM_001304286.1:c.-153G>T	NP_001291215.1:n.-153G>T
XM_011525160.1:c.-153G>T	XP_011523462.1:n.-153G>T
XM_011525161.1:c.-153G>T	XP_011523463.1:n.-153G>T
XM_011525162.1:c.-153G>T	XP_011523464.1:n.-153G>T
XM_011525163.1:c.-153G>T	XP_011523465.1:n.-153G>T
XM_011525164.1:c.-153G>T	XP_011523466.1:n.-153G>T
XM_011525162.2:c.-153G>T	XP_011523464.1:n.-153G>T
XM_011525163.2:c.-153G>T	XP_011523465.1:n.-153G>T
NM_000458.4:c.-153G>T MANE Select	NP_000449.1:n.-153G>T
NM_001165923.4:c.-153G>T	NP_001159395.1:n.-153G>T
NM_001304286.2:c.-153G>T	NP_001291215.1:n.-153G>T