Canonical Allele Identifier: CA431419593
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925103C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060381C>G , CM000664.2:g.219060381C>G GRCh38
NC_000002.11:g.219925103C>G , CM000664.1:g.219925103C>G GRCh37
NC_000002.10:g.219633347C>G NCBI36
NG_016741.1:g.5136G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.87G>C MANE Select ENSP00000295731.5:p.Gly29=
ENST00000295731.6:c.87G>C ENSP00000295731.5:p.Gly29=
NM_002181.3:c.87G>C NP_002172.2:p.Gly29=
NM_002181.4:c.87G>C MANE Select NP_002172.2:p.Gly29=
Search 100 bp 5'
Search 100 bp 3'