Canonical Allele Identifier: CA65951003
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs902605867
MyVariant Identifiers: chr2:g.219924807G>C (hg19) chr2:g.219060085G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060085G>C , CM000664.2:g.219060085G>C GRCh38
NC_000002.11:g.219924807G>C , CM000664.1:g.219924807G>C GRCh37
NC_000002.10:g.219633051G>C NCBI36
NG_016741.1:g.5432C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.315+68C>G MANE Select ENSP00000295731.5:n.315+68C>G
ENST00000295731.6:c.315+68C>G ENSP00000295731.5:n.315+68C>G
NM_002181.3:c.315+68C>G NP_002172.2:n.315+68C>G
NM_002181.4:c.315+68C>G MANE Select NP_002172.2:n.315+68C>G
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