Canonical Allele Identifier: CA350637780
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs761363200
MyVariant Identifiers: chr2:g.219925170C>G (hg19) chr2:g.219060448C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060448C>G , CM000664.2:g.219060448C>G GRCh38
NC_000002.11:g.219925170C>G , CM000664.1:g.219925170C>G GRCh37
NC_000002.10:g.219633414C>G NCBI36
NG_016741.1:g.5069G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.20G>C MANE Select ENSP00000295731.5:p.Arg7Pro
ENST00000295731.6:c.20G>C ENSP00000295731.5:p.Arg7Pro
NM_002181.3:c.20G>C NP_002172.2:p.Arg7Pro
NM_002181.4:c.20G>C MANE Select NP_002172.2:p.Arg7Pro
Search 100 bp 5'
Search 100 bp 3'