Canonical Allele Identifier: CA2733321989

Gene: HNF1B

Linked Data

• dbSNP Id: rs2033276275

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37720524T>C , CM000679.2:g.37720524T>C	GRCh38
NC_000017.10:g.36080519T>C , CM000679.1:g.36080519T>C	GRCh37
NC_000017.9:g.33154632T>C	NCBI36
NG_013019.2:g.29583A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000617811.5:c.1046-9861A>G MANE Select	ENSP00000480291.1:n.1046-9861A>G
ENST00000613727.4:c.968-9861A>G	ENSP00000477524.1:n.968-9861A>G
ENST00000614313.4:c.1046-9861A>G	ENSP00000482529.1:n.1046-9861A>G
ENST00000617272.4:c.1046-9861A>G	ENSP00000478682.1:n.1046-9861A>G
ENST00000617811.4:c.1046-9861A>G	ENSP00000480291.1:n.1046-9861A>G
ENST00000621123.4:c.968-9861A>G	ENSP00000482711.1:n.968-9861A>G
NM_000458.3:c.1046-9861A>G	NP_000449.1:n.1046-9861A>G
NM_001165923.3:c.968-9861A>G	NP_001159395.1:n.968-9861A>G
NM_001304286.1:c.968-9861A>G	NP_001291215.1:n.968-9861A>G
XM_011525160.1:c.1046-9861A>G	XP_011523462.1:n.1046-9861A>G
XM_011525161.1:c.1046-9861A>G	XP_011523463.1:n.1046-9861A>G
XM_011525164.1:c.968-9861A>G	XP_011523466.1:n.968-9861A>G
XR_934718.1:n.2236-3341T>C
XM_011525162.2:c.*323A>G	XP_011523464.1:n.*323A>G
XR_001752875.1:n.574+3038T>C
NM_000458.4:c.1046-9861A>G MANE Select	NP_000449.1:n.1046-9861A>G
NM_001165923.4:c.968-9861A>G	NP_001159395.1:n.968-9861A>G
NM_001304286.2:c.968-9861A>G	NP_001291215.1:n.968-9861A>G