×
SERVICES INTERRUPTION:
2026-08-07T10:00:00-0500
—
2026-08-14T18:00:00-0500
Allele Registry, ERepo, and Actionability UI services may experience intermittent service interruptions during this period.
ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA1329042645
Community Standard Title: NM_002181.4(IHH):c.137C= (p.Pro46=)
Gene: IHH
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.219060331G= , CM000664.2:g.219060331G=
GRCh38
NC_000002.11:g.219925053G= , CM000664.1:g.219925053G=
GRCh37
NC_000002.10:g.219633297G=
NCBI36
NG_016741.1:g.5186C=
Transcript Alleles
HGVS
Amino-acid Change
NM_002181.4:c.137C=
MANE Select
NP_002172.2:p.Pro46=
ENST00000295731.7:c.137C=
MANE Select
ENSP00000295731.5:p.Pro46=
NM_002181.3:c.137C=
NP_002172.2:p.Pro46=
ENST00000295731.6:c.137C=
ENSP00000295731.5:p.Pro46=
Search 100 bp 5'
Search 100 bp 3'