Canonical Allele Identifier: CA916778810

Gene: IHH

Linked Data

• dbSNP Id: rs1574689439

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219060365_219060366insACGCAAACTCGTG , CM000664.2:g.219060365_219060366insACGCAAACTCGTG	GRCh38
NC_000002.11:g.219925087_219925088insACGCAAACTCGTG , CM000664.1:g.219925087_219925088insACGCAAACTCGTG	GRCh37
NC_000002.10:g.219633331_219633332insACGCAAACTCGTG	NCBI36
NG_016741.1:g.5151_5152insCACGAGTTTGCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295731.7:c.102_103insCACGAGTTTGCGT MANE Select	ENSP00000295731.5:p.Gly35HisfsTer?
ENST00000295731.6:c.102_103insCACGAGTTTGCGT	ENSP00000295731.5:p.Gly35HisfsTer?
NM_002181.3:c.102_103insCACGAGTTTGCGT	NP_002172.2:p.Gly35HisfsTer?
NM_002181.4:c.102_103insCACGAGTTTGCGT MANE Select	NP_002172.2:p.Gly35HisfsTer?