Canonical Allele Identifier: CA350637262
Gene: IHH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060316T>C , CM000664.2:g.219060316T>C GRCh38
NC_000002.11:g.219925038T>C , CM000664.1:g.219925038T>C GRCh37
NC_000002.10:g.219633282T>C NCBI36
NG_016741.1:g.5201A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.152A>G MANE Select ENSP00000295731.5:p.Gln51Arg
ENST00000295731.6:c.152A>G ENSP00000295731.5:p.Gln51Arg
NM_002181.3:c.152A>G NP_002172.2:p.Gln51Arg
NM_002181.4:c.152A>G MANE Select NP_002172.2:p.Gln51Arg