Canonical Allele Identifier: CA350637563
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925105C>A (hg19) chr2:g.219060383C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060383C>A , CM000664.2:g.219060383C>A GRCh38
NC_000002.11:g.219925105C>A , CM000664.1:g.219925105C>A GRCh37
NC_000002.10:g.219633349C>A NCBI36
NG_016741.1:g.5134G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.85G>T MANE Select ENSP00000295731.5:p.Gly29Trp
ENST00000295731.6:c.85G>T ENSP00000295731.5:p.Gly29Trp
NM_002181.3:c.85G>T NP_002172.2:p.Gly29Trp
NM_002181.4:c.85G>T MANE Select NP_002172.2:p.Gly29Trp
Search 100 bp 5'
Search 100 bp 3'