Canonical Allele Identifier: CA1329042727
Gene: IHH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060480_219060481delinsCG , CM000664.2:g.219060480_219060481delinsCG GRCh38
NC_000002.11:g.219925202_219925203delinsCG , CM000664.1:g.219925202_219925203delinsCG GRCh37
NC_000002.10:g.219633446_219633447delinsCG NCBI36
NG_016741.1:g.5036_5037delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-14_-13delinsCG MANE Select ENSP00000295731.5:n.-14_-13delinsCG
NM_002181.3:c.-14_-13delinsCG NP_002172.2:n.-14_-13delinsCG
NM_002181.4:c.-14_-13delinsCG MANE Select NP_002172.2:n.-14_-13delinsCG