Canonical Allele Identifier: CA431419828
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925178G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060456G>A , CM000664.2:g.219060456G>A GRCh38
NC_000002.11:g.219925178G>A , CM000664.1:g.219925178G>A GRCh37
NC_000002.10:g.219633422G>A NCBI36
NG_016741.1:g.5061C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.12C>T MANE Select ENSP00000295731.5:p.Ala4=
ENST00000295731.6:c.12C>T ENSP00000295731.5:p.Ala4=
NM_002181.3:c.12C>T NP_002172.2:p.Ala4=
NM_002181.4:c.12C>T MANE Select NP_002172.2:p.Ala4=
Search 100 bp 5'
Search 100 bp 3'