Canonical Allele Identifier: CA764946515
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs1402273134
MyVariant Identifiers: chr2:g.219925188_219925189del (hg19) chr2:g.219060466_219060467del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060466_219060467del , CM000664.2:g.219060466_219060467del GRCh38
NC_000002.11:g.219925188_219925189del , CM000664.1:g.219925188_219925189del GRCh37
NC_000002.10:g.219633432_219633433del NCBI36
NG_016741.1:g.5050_5051del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.1_2del MANE Select ENSP00000295731.5:p.Met1ValfsTer?
ENST00000295731.6:c.1_2del ENSP00000295731.5:p.Met1ValfsTer?
NM_002181.3:c.1_2del NP_002172.2:p.Met1ValfsTer?
NM_002181.4:c.1_2del MANE Select NP_002172.2:p.Met1ValfsTer?
Search 100 bp 5'
Search 100 bp 3'