Canonical Allele Identifier: CA764946545
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1388050836
MyVariant Identifiers: chr2:g.219925199_219925200insC (hg19) chr2:g.219060477_219060478insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060480dup , CM000664.2:g.219060480dup GRCh38
NC_000002.11:g.219925202dup , CM000664.1:g.219925202dup GRCh37
NC_000002.10:g.219633446dup NCBI36
NG_016741.1:g.5039dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.-11dup MANE Select ENSP00000295731.5:n.-11dup
NM_002181.3:c.-11dup NP_002172.2:n.-11dup
NM_002181.4:c.-11dup MANE Select NP_002172.2:n.-11dup
Search 100 bp 5'
Search 100 bp 3'