Canonical Allele Identifier: CA350637557

Gene: IHH

Linked Data

• MyVariant Identifiers: chr2:g.219925104C>A (hg19) ; chr2:g.219060382C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219060382C>A , CM000664.2:g.219060382C>A	GRCh38
NC_000002.11:g.219925104C>A , CM000664.1:g.219925104C>A	GRCh37
NC_000002.10:g.219633348C>A	NCBI36
NG_016741.1:g.5135G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295731.7:c.86G>T MANE Select	ENSP00000295731.5:p.Gly29Val
ENST00000295731.6:c.86G>T	ENSP00000295731.5:p.Gly29Val
NM_002181.3:c.86G>T	NP_002172.2:p.Gly29Val
NM_002181.4:c.86G>T MANE Select	NP_002172.2:p.Gly29Val