Canonical Allele Identifier: CA431419562
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs2106310668
MyVariant Identifiers: chr2:g.219925097A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060375A>C , CM000664.2:g.219060375A>C GRCh38
NC_000002.11:g.219925097A>C , CM000664.1:g.219925097A>C GRCh37
NC_000002.10:g.219633341A>C NCBI36
NG_016741.1:g.5142T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.93T>G MANE Select ENSP00000295731.5:p.Gly31=
ENST00000295731.6:c.93T>G ENSP00000295731.5:p.Gly31=
NM_002181.3:c.93T>G NP_002172.2:p.Gly31=
NM_002181.4:c.93T>G MANE Select NP_002172.2:p.Gly31=
Search 100 bp 5'
Search 100 bp 3'